DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1

DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1 is an FDA 510(k)-cleared medical device (K973873) manufactured by American Telecare, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 28, 1997. Regulation: 8.