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Home >> News >> Articles >> FDA approves remote patient-monitoring system

FDA approves remote patient-monitoring system

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St Paul, MN - The Food and Drug Administration (FDA) has granted market approval for a remote patient-monitoring system, which allows physicians to instantly communicate with their implanted cardioverter defibrillator (ICD) patients, even if the two are miles apart, St Jude Medical announced.

The company's Housecall PlusTM system enables a physician to monitor transmissions in real time, in contrast to other remote ICD-monitoring systems, which allow only the review of stored data. The transmitter on the patient side, the size of an answering machine, connects to a telephone line and an electrical outlet and communicates with the receiver at the physician's office, transmitting "up-to-the-second information" on cardiac parameters and ICD functioning. The physician can remotely review real-time and stored electrograms, surface ECGs, and delivered therapies, according to St Jude.

Complete informations and data are available on the original website TheHeart.org




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