FDA 510(k), K973873, DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1

FDA 510(k), K973873, DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1

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510(K) Number: K973873
Device Name: DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1
Manufacturer: AMERICAN TELECARE, INC.
Device Classification Name: transmitters and receivers, physiological signal, radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 10/10/1997
Decision Date: 12/29/1997
Regulation Medical Specialty: Cardiovascular
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