Abstract: Stylet including a stylet knob, a stylet wire, and a swaged stylet wire retaining sleeve over the stylet wire which engages within the stylet knob providing for controlled length and straightness of the stylet wire and mating within the long thin walled stylet knob.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overridden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signals.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overridden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signlas.

Abstract: Lead connector for use between an external pulse generator and a pacing lead. The lead connector includes elongated geometrical spaced connector pins which plug into connector terminals of the pulse generator and a hole accepting the connector end of the pacing lead. A case of the lead connector supports a pressure plate which is spring biased against a thumbscrew and engages a connector of the pacing lead against the connector pins of the lead connector.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overriden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signals.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overridden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signals.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overridden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signals.

Abstract: A programmable cardiac pacemaker pulse generator utilizing digital circuitry for controlling the provision of cardiac stimulating pulses. The pulse generator is capable of having the rate, the pulse width, the pulse amplitude, the refractory period, the sensitivity and the mode of operation programmed. In addition, the pulse generator can have the output inhibited and can respond to programming signals causing a threshold margin test to be performed, effects of closure of the reed switch overridden, a hysteresis function added and a high rate exceeding the normal upper rate limit programmed. Many of the programmable functions of the pulse generator can either be programmed on a permanent or a temporary basis. The pulse generator further includes means for signaling the acceptance of a programming signal, and means to reset the program acceptance circuit if extraneous signals are detected as programming signals.

Abstract: There is disclosed herein a wristwatch size cardiac monitoring apparatus which is worn on the wrist of one arm. A conductive material housing acts as one electrode when held firmly in contact with the wrist of the arm on which it is worn. A finger of the other limb is placed on a receiving electrode of the casing which acts as the second electrode. Together, these two electrodes provide a Lead I electrocardiac signal to electronics within the housing. The second electrode consists of a metal layer on which is placed a dielectric material and when the finger is placed on top of the dielectric material, a capacitor is formed and the electric signal on the finger is transferred to the metal layer. Additionally, there is described circuitry which is used to operate the rate monitor. This circuitry includes means for detecting a QRS complex and for causing a count in beats per minute to be displayed, manifesting the heartbeat rate.

Abstract: There is disclosed herein a wristwatch size cardiac monitoring apparatus which is worn on the wrist of one arm. A conductive material housing acts as one electrode when held firmly in contact with the wrist of the arm on which it is worn. A finger of the other limb is placed on a receiving electrode of the casing which acts as the second electrode. Together, these two electrodes provide a Lead I electrocardiac signal to electronics within the housing. The second electrode consists of a metal layer on which is placed a dielectric material and when the finger is placed on top of the dielectric material, a capacitor is formed and the electric signal on the finger is transferred to the metal layer. Additionally, there is described circuitry which is used to operate the rate monitor. This circuitry includes means for detecting a QRS complex and for causing a count in beats per minute to be displayed, manifesting the heartbeat rate.

Abstract: A body-implantable, lead affixed with a pin or pins at its proximal end adapted to be connected to a pulse generator and with an electrode or electrodes at its distal end electrically connected via conductor means and adapted to be securely and permanently attached to a body organ. Electrode means in the form of an elongated member having a circumferential electrode formed on one end thereof and an opening passing therethrough from its proximal to distal end is affixed to the distal end of the conductor means. Tissue securing means are located within a chamber beyond the opening of the electrode body to protect body tissue while the lead is being moved to the desired location. The tissue securing means is then extendable out of the distal end of the electrode means to secure the electrode means in firm engagement with body tissue at the desired location.

Abstract: A sizing gauge for determining the proper size of heart valve for implantation in a natural heart valve orifice. The sizing gauge includes a handle which can be gripped by a surgeon, a sizing ring having a smooth outer surface and a hollow interior, and connecting struts connecting the sizing ring and the handle. The connecting struts is so constructed and arranged as to afford direct visual observation by the surgeon of heart tissue beyond the sizing ring when the latter is inserted in a heart orifice. Outer surfaces of the connecting struts diverge forwardly for connection to the sizing ring and merge with the outer surface of the sizing ring to permit the latter to be eased outwardly through the natural heart valve orifice.

Abstract: A gamma ray scintillation camera generating (X,Y) spatial coordinate and Z energy signals relative to detected radiation events. The camera signals are converted to their digital equivalents subsequent to which the apparent coordinate locations of detected events as determined by the camera are corrected to their true spatial coordinates based upon correction information stored in the system. In addition to spatial coordinate correction, the system provides for calibration of the camera Z signal response as a function of camera face location.

Abstract: An implantable heart valve including a suturing ring within which the body of the valve may be rotatably positioned following surgical implantation. The suturing ring is held to the valve body by binding means, such as an annular band or series of cord wraps. In one embodiment, the binding means may be heat-relaxed after the suturing ring has been bound to the valve body, thereby facilitating rotation of the valve body in the suturing ring. Slip ring means may be interposed between the suturing ring and the valve body to facilitate rotation. The slip ring means may be shaped to permit the binding means to hold the suturing ring tightly at its edges to the valve body to prevent the suturing ring from separating from the valve body at their mutually adjacent edges. The slip ring means may comprise a single ring or a pair of concentric slip rings having a mutual low-friction interface.

Abstract: A fluid dispensing instrument and method for placing a drug material into the canals of the Fallopian tubes of a female. The instrument has a housing carrying a piston and cylinder assembly. An elongated flexible tubular probe attached to the housing carries an expandable sleeve. The piston and cylinder assembly is operable to fully collapse the sleeve prior to insertion through the cervical opening into the uterine cavity. After the sleeve is inserted into the uterine cavity, an ampulla storing the drug material is loaded into the instrument. The piston and cylinder assembly is then actuated to initially partially expand the sleeve. Operation of the piston and cylinder assembly moves a plunger into the ampulla to dispense the drug material into the uterine cavity above the partly expanded balloon. The sleeve is then fully expanded to move the drug material from the uterine cavity into the canals of the Fallopian tubes.

Abstract: A body implantable, intravascular lead affixed with a pin or pins at its proximal end adapted to be connected to a pulse generator and with an electrode or electrodes at its distal end adapted to be placed in contact with the endocardium. An electrical conductor(s) encased within a nonconductive material substantially inert to body fluids and tissues electrically connects the electrode(s) with the pin(s) and is comprised of a first length of resilient conductor having a first flexibility and an axial mechanical loading characteristic and a second length of the conductor having a second flexibility greater than the first flexibility and incapable of sustaining the axial mechanical loading characteristic. A dumbbell shaped electrode body provides sufficient size and weight to maintain the distal end of the lead in the apex of the right ventricle.

Abstract: A dispensing instrument and method for simultaneously injecting fluids, as drug materials, into the canals of the Fallopian tubes of a female primate. The dispensing instrument has a body accommodating a container for storing the drug materials. An elongated member carrying an expandable balloon is mounted on the body. A sheath encloses the elongated member and balloon. The sheath is attached to a tubular needle which extends through the elongated member. A releasable lock holds both the sheath and needle in assembled relation with the body. A plunger moves the container into dispensing relation with the needle whereby the fluid in the container is carried via the needle into the uterine cavity. The fluid flows into the canals of the Fallopian tubes. The expandable member is subjected to fluid under pressure. The fluid is continuously monitored to maintain a continuous and uniform low pressure on the expanded balloon.

Abstract: A dispensing apparatus for placing a settable, fluid-like material in the uterine cavity and moving the material from the uterine cavity into the Fallopian tubes of a female. An elongated probe carries an expandable member, and a housing connected to the probe has a piston and cylinder structure and a container for storing the material. Material and expansion drive mechanisms are connected to an actuator selectively controlled by an operator. By operating the actuator or control means, the operator causes the material to be dispensed into the uterine cavity while at the same time sealing the cervical entrance to the cavity, and causing the expansion means to fully expand to conform to the shape of the uterine cavity and force the dispensed materials into the canals of the Fallopian tubes.

Abstract: Pulse generating apparatus which provides electrical heart-stimulating pulses only in the absence of normal heart activity. If the patient's heart has developed a life threatening arrhythmic condition the inventive apparatus automatically applies an electrical shock to the heart having sufficient magnitude to restore normal heart activity. The inventive apparatus features a redundant heartbeat sensing system which monitors two dynamic characteristics of heart function, for example, heart contraction and EKG. An electrical heart stimulating pulse is delivered to the patient's heart following the elapse of a specified period of time since the sensing of a dynamic characteristic indicative of a normal functional heart. Sensing control is automatically regained following successful heart stimulation, thereby inhibiting the application of further electrical pulses.

Abstract: Pulse generating apparatus which provides electrical heart-stimulating pulses only in the absence of normal heart activity. If the patient's heart has developed a life threatening arrhythmic condition the inventive apparatus automatically applies an electrical shock to the heart having sufficient magnitude to restore normal heart activity. The inventive apparatus features a redundant heartbeat sensing system which monitors two dynamic characteristics of heart function, for example, heart contraction and EKG. An electrical heart stimulating pulse is delivered to the patient's heart following the elapse of a specified period of time since the sensing of a dynamic characteristic indicative of a normal functional heart. Sensing control is automatically regained following successful heart stimulation, thereby inhibiting the application of further electrical pulses.