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FDA 510(k) K964554, PERSONAL TELEMEDICINE MODULE, by American Telecare, Inc.

FDA 510(k) K964554, PERSONAL TELEMEDICINE MODULE, by American Telecare, Inc.

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510(K) Number: K964554
Device Name: PERSONAL TELEMEDICINE MODULE
Manufacturer: American Telecare, Inc.
Device Classification Name: transmitters and receivers, physiological signal, radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 11/13/1996
Decision Date: 12/17/1996
Regulation Medical Specialty: Cardiovascular
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