Abstract: A mode switch control system for a hybrid transmission for a powertrain, the powertrain including an engine, a first motor/generator, and a second motor/generator, which controls a mode switch from a high speed mode to a low speed mode. The high speed mode is established by engaging a high-mode clutch. The low speed mode is established by engaging a low-mode brake. In the mode switch, the mode switch control system reduces the torque capacity of the high-mode clutch to zero linearly in time by an open-loop control system, and varies the torque of the second motor/generator to a target torque by a feedback control system so as to adjust the gear ratio to a target gear ratio, while the mode switch control system holds substantially constant the input torque from the engine, and the torque of the first motor/generator, to hold substantially constant the output torque.

Abstract: A lock-up clutch control device, which controls a lock-up clutch (6) installed in a torque converter (5) interposed between an engine (3) and a transmission (4) used with a vehicle, is disclosed. The lock-up clutch control device has a differential pressure generating device (7,8) which engages or disengages the lock-up clutch by adjusting a differential pressure supplied to the lock-up clutch, a sensor (13) which detects a vehicle speed, and a controller.

Abstract: An engine torque control device is configured to provide increase engine output torque during shifting, with excessive engine output torque being prevented while shift shock is reduced. The engine torque control device has an automatic transmission control section that controls an automatic transmission and an engine output torque control section that performs a torque increasing control of an engine output torque to increase the engine output torque during a downshifting so that an actual engine speed will substantially approach a target speed. The allowable time for torque increasing control is set according to the amount of torque increase. If the increase in engine output torque is below a specified value at the point when the allowable time has elapsed, the torque increasing control is continued, but if the torque increase is at or above the specified value when the allowable time has elapsed, the torque increasing control is forcibly halted.

Abstract: A control apparatus for controlling a stepped automatic transmission of a vehicle having an output shaft and an input shaft which is to be connected to an engine of the vehicle through a clutch while a shifting action is being effected in the transmission. The control apparatus includes a torque vibration restrainer operable, upon completion of the shifting action in the transmission, to restrain a torque vibration which is generated in a power transmitting path of the vehicle. The torque vibration restrainer applies an inverted-phase torque vibration which is inverted in phase with respect to the generated torque vibration, to the power transmitting path, and/or place the clutch in its slipping state or released state, for restraining the generated torque vibration.

Abstract: A control system and control method for a swap-shift transmission having auxiliary and main gearsets wherein precise synchronization control of ratio changes of each gearset at the start and at the end of a swap-upshift progression is achieved using an adaptive control to adjust friction element pressure values and slip times for friction elements of each gearset, whereby shift synchronization is achieved throughout the operating life of the transmission.

Abstract: An exerciser has a base, a driving device, a supporting board and a control device. The driving device is mounted on the base and has a motor, two rotating axles, two shaking arms, two swinging shafts and two lateral arms. The motor is securely attached to the base. The rotating axles are rotatably mounted on the base and have an angle between the rotating axles to make the rotating axles to form a V-shaped arrangement on the base. The shaking arms are securely and respectively attached to the rotating axles. The swinging shafts are rotatably and respectively attached to the shaking arms. The lateral arms including a first lateral arm and a second lateral arm are respectively mounted on the swinging shafts. The supporting board is pivotally connected to the first lateral arm and is slidably connected to the second lateral arm.

Abstract: An exercise device which uses two generally opposing grips on guides to guide a user through circular movements for exercise of the human body. The grips may be movably mounted to side supports or a central base. Resistance to the user's movement of the grips may be added.

Abstract: Exercise apparatus for resistance training has a pulley with a user-adjustable camming profile for changing the load curve.

Abstract: A highly versatile exercise apparatuses is disclosed. More particularly, the invention relates to a cable crossover exercise apparatus including a central weight stack and opposed extension arms. The invention also relates to a functional lift exercise apparatus including a central weight stack and substantially parallel extension arms. The invention further relates to a cable type exercise apparatus employing a pulley assembly with a 4:1 load ratio.

Abstract: Tool-switching device for a machine for measuring coordinates wherein the tool is fastened on the tool-carrier and held by the action of elements exerting an axial force. The locking force is taken over symmetrically by the elements of a Boys connection, which increases the repeatability of the connection; in one embodiment, two pins or spheres are driven by a sliding bushing provided with two “V”-shaped slits or with two lateral gorges. In the subsequent embodiments, the pins are replaced by spheres, by levers or by a stirrup.

Abstract: A draining apparatus for collecting fluids from a container. This device consists essentially of a base and a rotational receptacle support, which holds and rotates, the container, which is to be drained. The container is held in a nearly horizontal position with the container opening oriented outward and is rotated at high speed so that sufficient centrifugal force is developed to empty the contents. The contents are emptied into a collector, which allows for convenient transfer to a second container using a syringe type plunger.

Abstract: A centrifuge of the type having an outer bowl and an inner rotor both of which are generally cylindrical and rotate in the same direction but at slightly different rates separates slurry fed into the interior of the rotor into solids and liquid. An auger flight on the outside surface of the rotor carries the solids along the annular channel between the outside of the rotor and the inside of the bowl. The slurry is fed into a chamber at one end of the rotor and through outlet holes in the sides of the rotor into the channel. An end plate of the chamber has a forwardly projecting domed central nose which extends into the flowing slurry. Transverse guide plates of the rotor act to engage the slurry and accelerate it into rotation with the rotor before escaping through the holes. The guide plates are shaped with curved angularly projecting ribs on the downstream side in front of the hole over which the slurry flows in a smooth path before exiting the hole.

Abstract: Systems, apparatus, components and methods are disclosed that allow the clinician to circumvent the pubic arch in instances where it interferes with insertion of instrumentation into the prostate or periprostatic tissue. The systems, apparatus and components disclosed herein employ structures, such as needles and trocars, of shape memory alloys, such as nickel-titanium (Ni—Ti) for the purpose of avoiding the pubic arch when accessing the prostate from the perineum.

Abstract: The invention involves enhancing brain function by stimulating the brain using magnetic fields. Applications of the new methods include improving the condition of individuals with cognitive disorders, such as depression, and studying the effects of neural stimulation using induced electric fields. These techniques can avoid deleterious effects of psychotropic pharmaceutical treatments, and provide a relatively safe, comfortable, inexpensive means of direct cranial stimulation.

Abstract: An infant care apparatus having a canopy movable with respect to an infant support for supporting an infant between a lower position enclosing the infant in an infant compartment and an upper position opening the infant compartment. The canopy has an opening and a door that can be closed to block the opening and opened to unblock the opening. A radiant heater is located in a fixed position above the infant support to direct infrared energy toward the infant support. When the canopy is in its lower position, a convective heating system warms the infant compartment. The door either closes as the canopy moves to its lower position or opens as the canopy moves to its upper position.

Abstract: A method and device for controlling the inflation of a prosthesis, particularly applicable to gastric implants. A liquid-containing bag is connected to a unit defining a transfer circuit under the control of the shutter and connected to an inflatable envelope, where the shutter is constituted by a non-return check valve closable and openable magnetically by remote control.

Abstract: A cardiac harness for treating a patient's heart includes elastic rows connected by a connector assembly. The connector assembly can have a specific pattern, or can be formed of elongated elastic material connecting all of the apices of adjacent rows. The connectors maintain proper spacing between rows or rings on the harness and provide longitudinal stability.

Abstract: A DVI circuit for generating a digital video signal in accordance with a display standard of a personal computer, etc. is provided for a processor device to which an electronic endoscope is connected. On the output side of the DVI circuit, a high vision system converter which is an adapter unit is connected as arbitrarily attached and removed using a connector. In the processor device, when the fixed state of a fixing screw is detected by a detection switch SW1, and it is determined that the power supply line connected using a connector to the high vision system converter is in the energized state, a live line processing circuit activates a signal line of the connector. Thus, the adapter unit can be easily attached and removed without turning off the processor device.

Abstract: An endoscope system comprises an electronic endoscope, a plurality of types of optical adapters, a control device, and a display device. The electronic endoscope includes an imaging unit. The plurality of types of optical adapters includes a predetermined observational optical system and is freely detachably attached to the distal section of the electronic endoscope. The observational optical system incorporated in each optical adapter includes an identification section with which the type of optical adapter is identified. The control device is electrically connected to the electronic endoscope.

Abstract: A method for evaluating sleep disorders in mammals and distributing control information related to the sleep disorders through electronic communication networks. The method includes acquiring analog information related to physiological signals through a mobile device from a mammal user. The mammal user is at a geographic location outside of a sleep laboratory staffed by trained technicians. The mobile device is coupled to a sensing device, which is coupled to monitoring region(s) of the mammal. The method includes converting the analog information into a digital format using a signal processing device and transmitting information related to the physiological signals in the digital format to one or more service computers through an electronic communications network. Each of the service computers is operably coupled to a health information service facility. The method determines if the mammal user has related control information at one of the health information service facilities.

Abstract: A method and apparatus for measuring the biological condition of an animal by acquiring and analyzing its biological signals are provided. The biological signals from skin temperature, a photoplenthysmogram (PPG), an electrocardiogram (ECG), electrodermal activity (EDA), an electromyogram (EMG), and an electrogastrogram (EGG) are detected using a biological signal detection unit which is attached to the animal's skin. Feature vectors, including the mean heart rate of the photoplenthysmogram and its standard deviation, the very low frequency, low frequency, and high frequency components of heart rate variability, the frequency and mean amplitude of skin conductance responses, and the mean and maximum skin temperatures, are extracted from the detected biological signals.

Abstract: A method of self treating a disease, such as diabetes, includes collecting in one or more databases data representing values of parameters that related to the self treatment. The data is processed to provide a plurality of alternate choices between two or more actions that may be taken and a corresponding value for each action is calculated. A computerized system may be employed to perform the above method and the system may include a computer readable medium for executing the method.

Abstract: Apparatus and method support a repetitive administration of a therapeutic treatment through a delivery unit during a neurological event, such as a seizure, of a nervous system disorder. The medical device system monitors signal data from a sensor and through an amplifier. A neurological event is detected by a medical device system using a detection algorithm. Consequently, a electrical stimulation pulse is applied to an electrode. During the delivery of the electrical stimulation pulse, the medical device system blanks signal data that is associated with the electrode. Subsequently, additional blanking is providing during a time interval in which signal artifacts may occur and the amplifier is stabilizing. The medical device system then collects signal data for the detection algorithm to stabilize. Subsequently, the medical device system collects additional signal data in order to obtain statistically meaningful data.

Abstract: A method and system for determining the fall risk of a patient is provided. The method includes the evaluation of a patient to determine whether the patient exhibits one or more intrinsic fall risk factors selected from a group consisting of confusion, depression, altered elimination, dizziness, male gender, antiepileptic/anticonvulsant prescriptions and benzodiazepine prescriptions. A specific point value is assigned to each of the intrinsic risk factors found to be exhibited by the patient. A mobility test is also performed on the patient to evaluate the patient's ability to rise from a seated position, and a specific mobility test point value is assigned to the patient based upon the patient's performance of the mobility test. Each intrinsic risk factor's specific point value is then summed together with the specific mobility test point value to achieve a total risk score, and the patient's fall risk is determined based on the total risk score.

Abstract: A portable, handheld device for measuring lung- and airway-specific respiratory parameters. The device defines a chamber in fluid communication with a mouthpiece. A sensor and/or a flow sensor monitor pressure and/or airflow within the device. A respiratory gas source, e.g., an internal pump, or an external compressor, is also in fluid communication with the chamber and a mouthpiece. The device operates in an active phase and a passive phase. In the active phase, a subject forcibly exhales into the device and the sensors collect spirometric data. In the passive phase, the pump is activated to pump air from the device and inflate the subject's lungs to a specific capacity. The sensors monitor pressure and/or flow as the air is introduced into the subject's respiratory system. The data collected by the sensor is used to determine lung and airway specific parameters, including but not limited to, airway conductance, airway resistance, airway compliance and total lung capacity.

Abstract: A target nerve or nerve plexus registration point is located utilizing a nerve stimulator needle positioned in a bore of a carrier. The carrier is configured with an electrically nonconductive smooth curved surface at a distal end of the bore. The needle tip is fixed in an operative cutaneous electrode position and the smooth curved surface of the carrier is forced against and compresses the epidermis, corium and subcutaneous tissue and traverses cutaneous surfaces to locate a target nerve or nerve plexus without physical penetration by the needle tip. The needle is then inserted at the located point, with or without the needle path being guided by the bore. In another embodiment, a subcutaneous portion of carrier is introduced and is pivoted about its introduction point to locate the target nerve.

Abstract: The invention provides systems, methods and a node accessing and anchoring device, comprising an elongated shaft, a tissue cutting member, at least one anchoring element extending from a position at or near the distal end of the shaft; and a radiation detector. The radiation detector is effective to locate and identify sentinel lymph nodes following injection of radioactive material into a primary lesion site within a patient. The tissue cutting member, which may be activated with radio frequency energy, is effective to allow access of the elongated shaft to a sentinel lymph node. The anchoring elements are effective to anchor the device to or adjacent a sentinel lymph node accessed by the device. Anchoring elements may assume radially, longitudinally, or mixed radially and longitudinally curved or coiled configurations when deployed.

Abstract: A physiotherapeutic apparatus includes a bed, a sliding mechanism, and a connecting rod combination; the bed has thereon a threaded rod, an actuating device for causing rotation of the threaded rod, and a circuit controller for controlling motion of the actuating device; the bed has two lateral rails, and a lengthways-extending rail, which are parallel to the threaded rod; the sliding mechanism has rolling wheels thereon, which fit in and roll along each one of the rails for increasing motion smoothness and steadiness, preventing tilting and reducing wear; a threaded sleeve is secured to the sliding mechanism and positioned around the threaded rod so that rotation of the threaded rod will cause forward and backward motion of the sliding mechanism; the connecting rod combination is foldable and used to fix a user's lower limbs, and it is pivoted to the bed and the sliding mechanism two ends thereof.

Abstract: A cosmetic device comprises a support member; a cap member attached to the support member and having a front face; a vibration actuator disposed inside the cap member, which produces vibration for providing massage effect on a skin; and an uneven surface member as an outermost layer covering at least the front face of the cap member. The uneven surface is configured to prevent denudation of a treatment agent applied on the skin.

Abstract: Disclosed is a skin care appliance capable of realizing various skin care modes using an oscillator vibrating up and down in the way of a magnetic coil, conducting the galvanic massage and the iontophoresis massage based on the oscillator, and making the magnetic-color-sound therapy. The skin care appliance includes a case with a predetermined shape, and a vibration unit installed within the case and having an oscillator. The oscillator oscillates in the way of a magnetic coil upon receipt of the power from a power supply unit. An outer electrode is charged to a polarity opposite to the polarity of the oscillator, and placed at the case. A switch unit is provided at the case. A control unit controls the vibration unit in accordance with the signals from the switch unit.

Abstract: A compression apparatus including an expandable body configured for disposal about a foot. A strap extends from the body. The strap is configured for disposal about the foot adjacent an ankle. The strap has a first layer configured to engage an outer surface of the foot adjacent the ankle, a second layer and a third cushion layer disposed therebetween. The body may include a metatarsal portion. The first layer and the second layer may be configured to provide a barrier to the third cushion layer. The first layer may be configured to prevent engagement of the third cushion layer with the outer surface of the foot.

Abstract: A device is disclosed for self administration of adjustable lumbar traction by a user in a supine position upon a support. The device comprises an upper body harness releasably encircling the torso and anchored to the support spacedly outwardly of the user's head, a lower body harness releasably encircling the user's waist and anchored to a support spacedly outwardly of the user's feet and user adjustable elastically biased tensioning members extending between the lower body harness and the support to which it is anchored. The device is preferably carried on a bedstead or table.

Abstract: A gravitational pressure regulating mechanism for use with a valve is provided for control of pressure and diversion of bodily fluids. The mechanism includes a reservoir having first and second ends, the first end being open and the second end having a floor and an entry port, and a free floating weight adapted to freely slide in the reservoir from a closed position wherein the weight is adjacent the floor to an opened position wherein the weight is positioned away from the floor. The weight has a closure member having a surface to engage the entry port when the weight is in the closed position. The mechanism further includes a cap having an exit port to seal the open first end of the reservoir. The mass of the weight is proportional to the amount of resistance to flow of the bodily fluids through the regulating mechanism.

Abstract: A multi lumen catheter including an inner tube having a front tip, an outer tube, a tube or lumen for inserting a guide wire, a blood extraction lumen and a blood return lumen which are formed in the outer tube and inner tube, respectively, or both in the outer tube, wherein the inner tube is inserted in the outer tube, and allowed to slide relative thereto, and the front tip is jointed to the front end of the outer tube to shut off communication of the lumens with the exterior. A multi-lumen catheter with balloon includes a balloon provided on a tabular body at a front end thereof, a blood return port and a blood extraction port provided in the tubular body on opposite sides of the balloon, and an outer cylinder slidable on the tubular body to close the blood extraction and blood return ports and the balloon.

Abstract: A safety syringe has a simple structure, is convenient to use, and has a low cost. The safety syringe includes a sliding casing, a needle, a syringe barrel, a piston, a latching casing, a spring and a plunger inside the syringe barrel. The safety syringe can be easily used to carry out an injection and has a safety mechanism that can be actuated using a single hand. The sliding casing can be automatically positioned and locked in two directions. This design guarantees that, during processing of the syringe after it is used, the needle's point is always protected by the sliding casing. The safey syringe is also auto-locking; after it has been used, the plunger is locked in the syringe barrel and cannot be pulled out any longer. Any attempt to use the syringe again will cause the plunger to be broken and the syringe to be damaged, thus ensuring a one-time use.

Abstract: A portable enteral feeding apparatus (20) facilitates ambulatory enteral feeding and prevents damage to an enteral feeding tube during use. The apparatus includes a backpack type enteral feeding support, a soft pouch (38) having a hook and loop surface on the pouch and a rigid spacer (68). The pouch surrounds the fluid container (42), trapping and attaching it to the inside of a backpack using hook and loop system. The soft sided pouch provides easy removal and replacement of a variety of fluid containers in a mobile backpack. The rigid spacer supports the pouch and provides clearance for connection to enteral feeding tubing (32). Shoulder straps (26) substantially immobilize the apparatus relative to a subject. A telescopic enteral feeding tube concealment belt (30) is provided that allows patient mobility while concealing and protecting enteral feeding tubes.

Abstract: An ingestible device for delivering a substance to a chosen location in the GI tract of a mammal includes a receiver of electromagnetic radiation for powering an openable part of the device to an opened position for dispensing of the substance. The receiver includes a coiled wire that couples the energy field, the wire having an air or ferrite core. In a further embodiment the invention includes an apparatus for generating the electromagnetic radiation, the apparatus including one or more pairs of field coils supported in a housing. The device optionally includes a latch defined by a heating resistor and a fusible restraint. The device may also include a flexible member that may serve one or both the functions of activating a transmitter circuit to indicate dispensing of the substance; and restraining of a piston used for expelling the substance.

Abstract: Embodiments of the present invention provide a method and system of treating intraocular pressure. Laser light is directed to the ciliary region of the target eye. The light stimulates the ciliary region and ablates debris lodged therein. An immune response may be triggered by the stimulation of the ciliary body. Intraocular pressure is reduced by the increase in aqueous flow from the anterior chamber in the eye permitted by the resultant removal of debris blocking the uveo-scleral outflow pathway.

Abstract: A device for moving a therapeutic energy source over an area to be treated including at least one therapeutic energy source adapted to produce therapeutic energy and coupled to a mounting structure, and at least one moving unit connected to the mounting structure and adapted to move the mounting structure and the energy source coupled thereto over an area to be exposed to therapeutic energy.

Abstract: In an electrosurgical generator for generating radio frequency power, the generator includes a radio frequency output stage having two or more output connections, and a power supply coupled to the output stage for supplying power to the output stage. A controller is operable to cause the generator to supply a blended output signal alternating constantly between a first output signal across the output connections in which the radio frequency output voltage developed across the output connections is limited to at least a first predetermined threshold value for cutting or vaporisation of tissue, and a second output signal across the output connections in which the radio frequency output voltage developed across the output connections is limited to a second threshold value for coagulation.

Abstract: A system for heat ablation of tissue in a patient comprises a plurality of electrodes operatively connected to a source of radiofrequency energy and configured to apply RF energy to tissue at a patient site, a plurality of RF current restricting circuits, each circuit coupled between one of the plurality of electrodes and the source of radiofrequency energy, and configured to restrict RF energy to the electrode when the current restricting circuit is enabled and not restrict RF energy to flow to the electrode when the current restricting circuit is disabled, at least one return electrode adapted to contact the patient and configured to return RF energy to the RF source; and a switching mechanism configured to selectively enable each of the plurality of RF current restricting circuits, in one of a sequential and non sequential fashion, wherein the switching mechanism is isolated from each of the current restricting circuits.

Abstract: The invention provides methods and devices to treat obesity by ablating tissue from an exterior surface of a stomach of a patient. For example, the invention may involve ablation of exterior stomach tissue to alter gastric myoelectric activity or muscle function from the exterior surface of the stomach to produce abnormal gastric peristalsis without damaging the mucosal lining of the stomach. The invention may further provide methods and devices to monitor the gastric myoelectric activity before and after the ablation procedure.

Abstract: Ablation probes are provided for perfusing the tissue, while the tissue is ablated. The ablation probe comprises an elongated shaft and an ablative element, such as a needle electrode. The ablation probe further comprises a lumen that extends through the probe shaft, which will be used to deliver a fluid to the distal end of the probe shaft for perfusion into the surrounding tissue. The ablation probe further comprises a porous structure that is associated with the distal end of the shaft in fluid communication with the lumen. For example, the distal end of the shaft, or the entirety of the shaft, can be composed of the porous structure. Or, if the ablative element is an electrode, the electrode can be composed of the porous structure. Because the pores within the porous structure are pervasive, the fluid will freely flow out into the tissue notwithstanding that some of the pores may become clogged.

Abstract: A unilateral external fixator device that allows for gross manipulation and fine adjustment of deformities in six degrees of freedom. The device may comprise a strut assembly and two compound movable joints, one at each end of the strut assembly. One compound movable joint may comprise two revolute joints, each containing a gear reduction mechanism and may rotate about the strut. The second compound movable joint may contain two revolute joints, each containing a gear reduction mechanism, and may move along the length of the strut assembly. The gear reduction mechanisms may comprise helical spline assemblies that allow for gross and fine adjustment of the fixator.

Abstract: A fixation plate includes a set of threaded peg holes adapted to individually receive fixation pegs therethrough and non-threaded alignment holes having a relatively smaller diameter than the peg holes and preferably sized to closely receive a K-wire. The alignment holes are located between the peg holes. One alignment hole is configured for aligning the plate during an osteotomy procedure, while other alignment holes are configured for use after fracture reduction and receive K-wires to temporarily stabilize the fracture and secure the plate to the bone and determine whether pegs inserted through adjacent respective peg holes will be properly located before drilling relatively larger holes for such pegs.

Abstract: The present invention provides a cut block for cutting the femur and tibia during knee replacement surgery.

Abstract: A medical retrieval instrument of the present invention includes a plurality of filaments for holding an object and a hollow section through which a first end of each of said plurality of filaments passes. The hollow section comprises a plurality of fixing sections for fixing a second end of each of said plurality of filaments, for example. The hollow section is arranged in a distal end portion of a sheath. The hollow section is inserted into the body cavity by the sheath and then holds an object such as renal calculus or ureteral calculus in the body cavity and retrieves them to outside the body.

Abstract: A medical system for approximating the esophageal sacs in an infant afflicted with esophageal atresia. The medical device includes an esophageal catheter and a gastric catheter. The distal end of the esophageal catheter, which includes a magnetic tip, is passed through the esophagus to the upper esophageal sac. The distal end of the gastric catheter, which also includes a magnetic tip, is passed through a gastrostomy and into the lower esophageal sac. The magnetic forces created by both magnets results in approximation of the esophageal sacs. Pressure-induced necrosis establishes a passageway between the esophageal sacs. A stent or stent-graft can be deployed within the established passageway to prevent re-synopsis of the esophagus.

Abstract: A single-use lancet device is provided for drawing capillary blood samples. The device includes a body having an upper portion and a lower portion and a trigger carried by the upper portion of the body. The trigger is movable between a first raised position wherein the device is cocked and a second depressed position wherein the device is fired. A needle assembly is provided which is movable between a cocked position and a striking position. A free-floating drive spring is provided for moving the needle assembly from its cocked position to its striking position. A bounceback spring is integrally molded with the needle assembly and includes a pair of generally V-shaped spring arms. A trigger bar has a first position wherein it holds the needle assembly in its cocked position, and the trigger bar has a second position wherein it allows the needle assembly to move to its striking position as the drive spring expands.

Abstract: A bleeding time testing system including a bleeding time tester having a cutting blade and a switch actuator, and a tripper affixed onto the body of the tester and cooperative with the switch actuator. The tripper includes a housing, a slide frame slidably interconnected to the housing and having a surface cooperative with the switch actuator, and an actuator button mounted on the housing and cooperative with the slide frame. The actuator button is positioned so as to cause the slide frame to move to the activated position when the actuator is moved downwardly. The actuator button is positioned directly above a centerline of the cutting blade of the tester.