Abstract: A method of operating a medical device comprises updating a regulatory approval status stored in at least one of the medical device or a second device operable to communicate with the medical device, and enabling or disabling the at least one function in the medical device based on the regulatory approval status. The regulatory approval status corresponds to at least one function performable by the medical device.

Abstract: This document describes, among other things, a method of operating a medical device comprising updating a regulatory approval status stored in at least one of the medical device or a second device operable to communicate with the medical device, and enabling or disabling the at least one function in the medical device based on the regulatory approval status. The regulatory approval status corresponds to at least one function performable by the medical device.

Abstract: This document describes, among other things, a method of operating a medical device comprising updating a regulatory approval status stored in at least one of the medical device or a second device operable to communicate with the medical device, and enabling or disabling the at least one function in the medical device based on the regulatory approval status. The regulatory approval status corresponds to at least one function performable by the medical device.

Abstract: Transthoracic cardiac stimulation therapies provide for detection and treatment of cardiac asystole subsequent to delivery of a defibrillation therapy. A pacing therapy is transthoracicly delivered to terminate detected cardiac asystole using residual energy from a defibrillation energy storage source. The residual energy usable for the pacing therapy is sufficient to transthoracicly deliver at least one pacing pulse, and is typically sufficient to deliver a series of pacing pulses, prior to depletion of the defibrillation energy storage source. Detection of cardiac asystole is performed following delivery of each pacing pulse, and subcutaneous pacing support is terminated in response to detecting cardiac asystole termination.

Abstract: This document describes, among other things, a method of operating a medical device comprising updating a regulatory approval status stored in at least one of the medical device or a second device operable to communicate with the medical device, and enabling or disabling the at least one function in the medical device based on the regulatory approval status. The regulatory approval status corresponds to at least one function performable by the medical device.

Abstract: An apparatus and method for delivering defibrillation shock therapy employing a multi-terminal pulse output circuit. In such a circuit, at least three electrode lead terminals are switchably connected to the positive and negative terminals of an energy storage capacitor. By serially switching selected electrode lead terminals to the capacitor terminals, a variety of shock pulse waveforms may be generated.

Abstract: A cardiac sensing and stimulation system includes a housing within which energy delivery circuitry and detection circuitry are provided. Subcutaneous electrodes are coupled to the energy delivery and detection circuitry and arranged in a non-contacting relationship with respect to cardiac tissue, great vessels, and coronary vasculature. A lead system is coupled to the energy delivery and detection circuitry. The lead system electrodes are configured to contact cardiac tissue, great vessels, or coronary vasculature. A controller, provided in the housing, is coupled to the energy delivery and detection circuitry. The controller configures the system to operate in a first mode using at least the subcutaneous electrodes, and to operate in a second mode using at least the lead electrodes. The controller can selectively switch between the first and second modes, and selectively enable and disable components and circuitry associated with the first and second modes and combinations of these modes.

Abstract: A reconfigurable cardiac device includes a housing, and detection circuitry and energy delivery circuitry provided in the housing. One or more subcutaneous, non-intrathoracic electrodes are coupled to the energy delivery and detection circuitry. A lead interface is provided on the housing and coupled to the energy delivery and detection circuitry. The lead interface is configured to receive at least one lead that includes one or more intrathoracic lead electrodes. A controller is provided in the housing and coupled to the lead interface and the energy delivery and detection circuitry. The system is operable in a first configuration using the subcutaneous electrodes in the absence of the lead and operable in a second configuration using at least one or more of the lead electrodes. The system is capable of providing cardiac activity sensing and stimulation in each of the first and second system configurations, respectively.

Abstract: Transthoracic cardiac stimulation therapies provide for detection and treatment of cardiac asystole subsequent to delivery of a defibrillation therapy. A pacing therapy is transthoracicly delivered to terminate detected cardiac asystole using residual energy from a defibrillation energy storage source. The residual energy usable for the pacing therapy is sufficient to transthoracicly deliver at least one pacing pulse, and is typically sufficient to deliver a series of pacing pulses, prior to depletion of the defibrillation energy storage source. Detection of cardiac asystole is performed following delivery of each pacing pulse, and subcutaneous pacing support is terminated in response to detecting cardiac asystole termination.

Abstract: An apparatus and method for delivering defibrillation shock therapy employing a multi-terminal pulse output circuit. In such a circuit, at least three electrode lead terminals are switchably connected to the positive and negative terminals of an energy storage capacitor. By serially switching selected electrode lead terminals to the capacitor terminals, a variety of shock pulse waveforms may be generated.

Abstract: A cardiac rhythm management system includes an electrosurgery mode of operating an implantable cardiac rhythm management device, such as a pacemaker, defibrillator, or pacer/defibrillator. In electrosurgery mode, certain device parameters are programmed to particular electrosurgery mode values in order to increase the immunity of the implanted device to electromagnetic interference during electrosurgery. Electrosurgery mode device parameter values include both previously-programmed values and different values that are particular to electrosurgery mode. Electrosurgery mode is initiated by an external programmer, which enables electrosurgery mode parameters, displays an indicator to the user, and disables further device parameter programming until electrosurgery mode is terminated by a user request from the external programmer. Electrosurgery mode includes asynchronous pacing, such as DOO mode providing atrial and ventricular pacing at previously programmed rate, AV delay, amplitudes, and pulse widths.

Abstract: An apparatus and method for delivering defibrillation shock therapy employing a multi-terminal pulse output circuit. In such a circuit, at least three electrode lead terminals are switchably connected to the positive and negative terminals of an energy storage capacitor. By serially switching selected electrode lead terminals to the capacitor terminals, a variety of shock pulse waveforms may be generated.

Abstract: An apparatus and method for delivering defibrillation shock therapy employing a multi-terminal pulse output circuit. In such a circuit, at least three electrode lead terminals are switchably connected to the positive and negative terminals of an energy storage capacitor. By serially switching selected electrode lead terminals to the capacitor terminals, a variety of shock pulse waveforms may be generated.

Abstract: Systems, structures, and methods are provided to share information in systems including implantable medical devices. Information acquired or generated in the systems is made available so that components of the systems or implantable medical devices can use it without having to reacquire such information.