RESTERIL. OF IMPLANT. ELECT. & ADAPTER

RESTERIL. OF IMPLANT. ELECT. & ADAPTER is an FDA 510(k)-cleared medical device (K772331) manufactured by Telectronics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on January 10, 1978. Regulation: 8.