Abstract: A submersible well pump assembly has a pump housing with a pump discharge on upper end. A pump barrel is located within the pump housing, defining an annular passage between the barrel and the pump housing. A plunger is reciprocally carried in the barrel. A motor mounted below the pump housing and operatively couples to the plunger causes the plunger to reciprocate between an upstroke and a down-stroke. A valve and porting arrangement directs well fluid in the barrel below the plunger into the annular passage and out the discharge during a down stroke of the plunger. The valve and porting arrangement admits well fluid into the barrel below the plunger during the up stroke of the plunger. A connecting rod extends between the motor and the plunger. The connecting rod is in tension during the down-stroke.

Abstract: An infusion system includes an infusion device and a sensing device. The infusion system may further include a characteristic determining device. The infusion device also includes a communication system for transmitting to and receiving communications from the sensing device or a computer. The sensing device may sense an analyte of a bodily fluid of the user. The analyte may be calibrated using data from the infusion device and from a characteristic determining device. The system may be set up to automatically call for assistance when analytes reach a certain level.

Abstract: An infusion system is for infusing a fluid into the body of a patient. The infusion system includes at least one sensor for monitoring blood glucose concentration of the patient and an infusion device for delivering fluid to the patient. The sensor produces at least one sensor signal input. The infusion device uses the at least one sensor signal input and a derivative predicted algorithm to determine future blood glucose levels. The infusion device delivers fluid to the patient when future blood glucose levels are in a patient's target range. The infusion device is capable of suspending and resuming fluid delivery based on future blood glucose levels and a patient's low shutoff threshold. The infusion device suspends fluid delivery when future blood glucose levels falls below the low shutoff threshold. The infusion device resumes fluid delivery when a future blood glucose level is above the low shutoff threshold.

Abstract: A submersible well pump assembly has a pump housing with a pump discharge on upper end. A pump barrel is located within the pump housing, defining an annular passage between the barrel and the pump housing. A plunger is reciprocally carried in the barrel. A motor mounted below the pump housing and operatively couples to the plunger causes the plunger to reciprocate between an upstroke and a down-stroke. A valve and porting arrangement directs well fluid in the barrel below the plunger into the annular passage and out the discharge during a down stroke of the plunger. The valve and porting arrangement admits well fluid into the barrel below the plunger during the up stroke of the plunger. A connecting rod extends between the motor and the plunger. The connecting rod is in tension during the down-stroke.

Abstract: An infusion system includes an infusion device and a sensing device. The infusion system may further include a characteristic determining device. The infusion device also includes a communication system for transmitting to and receiving communications from the sensing device or a computer. The sensing device may sense an analyte of a bodily fluid of the user. The analyte may be calibrated using data from the infusion device and from a characteristic determining device. The system may be set up to automatically call for assistance when analytes reach a certain level.

Abstract: An infusion system includes an infusion device and a sensing device. The infusion system may further include a characteristic determining device. The infusion device also includes a communication system for transmitting to and receiving communications from the sensing device or a computer. The sensing device may sense an analyte of a bodily fluid of the user. The analyte may be calibrated using data from the infusion device and from a characteristic determining device. The system may be set up to automatically call for assistance when analytes reach a certain level.

Abstract: An infusion system is for infusing a fluid into the body of a patient. The infusion system includes at least one sensor for monitoring blood glucose concentration of the patient and an infusion device for delivering fluid to the patient. The sensor produces at least one sensor signal input. The infusion device uses the at least one sensor signal input and a derivative predicted algorithm to determine future blood glucose levels. The infusion device delivers fluid to the patient when future blood glucose levels are in a patient's target range. The infusion device is capable of suspending and resuming fluid delivery based on future blood glucose levels and a patient's low shutoff threshold. The infusion device suspends fluid delivery when future blood glucose levels falls below the low shutoff threshold. The infusion device resumes fluid delivery when a future blood glucose level is above the low shutoff threshold.

Abstract: An infusion system is for infusing a fluid into the body of a patient. The infusion system includes at least one sensor for monitoring blood glucose concentration of the patient and an infusion device for delivering fluid to the patient. The sensor produces at least one sensor signal input. The infusion device uses the at least one sensor signal input and a derivative predicted algorithm to determine future blood glucose levels. The infusion device delivers fluid to the patient when future blood glucose levels are in a patient's target range. The infusion device is capable of suspending and resuming fluid delivery based on future blood glucose levels and a patient's low shutoff threshold. The infusion device suspends fluid delivery when future blood glucose levels falls below the low shutoff threshold. The infusion device resumes fluid delivery when a future blood glucose level is above the low shutoff threshold.

Abstract: An external infusion device for delivering insulin from a reservoir into a body of a user includes the capability to deliver time-shifted basal insulin. The external infusion device includes at least one drive mechanism operatively couplable to the reservoir to deliver insulin into the body of the user, at least one processor to control the external infusion device, at least one power supply, at least one display device operatively coupled to the processor to provide visual information to the user, at least one input device operatively coupled to the processor to allow the user to command the processor, and a housing. Time-shifting of basal insulin occurs when a portion of basal insulin is added to a bolus, to a current basal rate, or to a bolus and a current basal rate.

Abstract: A monitor device for a fluid infusion system and its operating, display, and data processing characteristics are described herein. One embodiment of the monitor device is used in an insulin infusion system having an insulin infusion pump and a continuous glucose sensor transmitter. The monitor device is configured as a wireless bedside monitor that wirelessly receives status data from a device in the fluid infusion system, such as the infusion pump or the sensor transmitter. The monitor device supports a number of user interface features, alarm/alert features, and graphical display features, where such features enhance the overall operation and user-friendliness of the monitor device. For example, the monitor device can generate status icons that graphically indicate the time remaining for an exhaustible operating quantity of a device in the infusion system (e.g., a battery charge, a fluid reservoir volume, or a calibration or replacement period).

Abstract: An infusion system is for infusing a fluid into the body of a patient. The infusion system includes at least one sensor for monitoring blood glucose concentration of the patient and an infusion device for delivering fluid to the patient. The sensor produces at least one sensor signal input. The infusion device uses the at least one sensor signal input and a derivative predicted algorithm to determine future blood glucose levels. The infusion device delivers fluid to the patient when future blood glucose levels are in a patient's target range. The infusion device is capable of suspending and resuming fluid delivery based on future blood glucose levels and a patient's low shutoff threshold. The infusion device suspends fluid delivery when future blood glucose levels falls below the low shutoff threshold. The infusion device resumes fluid delivery when a future blood glucose level is above the low shutoff threshold.

Abstract: According to one embodiment, a programmable medical device includes a storage means for storing a plurality of software modules operable to control one or more medical functions of the device. The device is configured to receive a plurality of commands. An operational state of each of the software modules is configured to be controlled according to a respective one of the commands.

Abstract: An infusion system is for infusing a fluid into the body of a patient. The infusion system includes at least one sensor for monitoring blood glucose concentration of the patient and an infusion device for delivering fluid to the patient. The sensor produces at least one sensor signal input. The infusion device uses the at least one sensor signal input and a derivative predicted algorithm to determine future blood glucose levels. The infusion device delivers fluid to the patient when future blood glucose levels are in a patient's target range. The infusion device is capable of suspending and resuming fluid delivery based on future blood glucose levels and a patient's low shutoff threshold. The infusion device suspends fluid delivery when future blood glucose levels falls below the low shutoff threshold. The infusion device resumes fluid delivery when a future blood glucose level is above the low shutoff threshold.

Abstract: A monitor device for a fluid infusion system and its operating, display, and data processing characteristics are described herein. One embodiment of the monitor device is used in an insulin infusion system having an insulin infusion pump and a continuous glucose sensor transmitter. The monitor device is configured as a wireless bedside monitor that wirelessly receives status data from a device in the fluid infusion system, such as the infusion pump or the sensor transmitter. The monitor device supports a number of user interface features, alarm/alert features, and graphical display features, where such features enhance the overall operation and user-friendliness of the monitor device. For example, the monitor device can generate status icons that graphically indicate the time remaining for an exhaustible operating quantity of a device in the infusion system (e.g., a battery charge, a fluid reservoir volume, or a calibration or replacement period).

Abstract: The invention is a motorized linkage for operating a door strike. A six volt power source, controlled by a security code, rotates a small electric motor when a proper security code is given. The motor rotates a shaft which engages a coil spring. This moves a locking cam. When a catch on the locking cam separates from the locking lever catch, the latch bolt keeper may be manipulated by a user.

Abstract: An aqueous size composition for glass fibers is disclosed which includes a thermoplastic polymer resin powder, a coupling agent, and fugitive processing aids, such as binders or film formers. The composition is applied to the glass fiber surfaces during the fiber forming process. A fugitive rheology modifier material may be added to the size composition. One embodiment of the composition includes a polyethylene oxide binder material and a polyphenylene sulfide thermoplastic polymer resin.

Abstract: A method for impregnating a strand of filaments during the strand manufacture with thermoplastic or thermoset polymer powder particles is disclosed. The method includes the steps of forming a strand of filaments, keeping the filaments separate, impregnating the filaments with an aqueous slurry containing the powder particles, and drying the filaments to remove the water and produce a strand impregnated with powder particles. The powder particles are present on the strand in an amount of between about 5 to 50 weight percent based on the weight of the impregnated strand. Glass fibers coated with the slurry according to the process of this invention are suitable for impregnation with thermoplastic powders.

Abstract: An aqueous size composition for glass fibers is disclosed which includes a coupling agent, a binder or film former material and a thermoplastic polymer resin powder, wherein said composition is applied to the glass fiber surfaces during the fiber forming process. A rheology modifier material may be added to the size composition. One embodiment of the composition includes an organosilane coupling agent, a polyethylene oxide binder material and a polyamide thermoplastic polymer resin.

Abstract: A thermoplastic impregnated fiberglass pipe or tube and the process for making such pipe are disclosed. The pipe or tube is made of thermoplastic impregnated fibrous roving which consists of a plurality of glass filaments, at least a portion of the filaments' surfaces being in contact with the residue produced by evaporating water from an aqueous size composition consisting of an organosilane coupling agent, a polyethylene oxide binder material, and a polypropylene thermoplastic polymer resin, wherein the composition is applied to the glass fiber during the fiber forming process. The pipe forming process includes filament winding the rovings around a spindle and thereafter heating the wound rovings to fuse the thermoplastic polymer resin.

Abstract: A mechanism for adjusting the height and viewing angle of a flat panel display which is viewed in conjunction with a portable personal computer. The mechanism includes a pair of arms that swing the display panel betwen the lowered and raised position, cooperating with a cam wheel moveable in a cam track. In a raised position, the flat panel display may be adjusted in viewing angle. In a lowered position the flat panel display may be securely latched to the portable personal computer to protect the display from damage.