MIKROS, MIKROS VS-1, PULSE GENERATOR

MIKROS, MIKROS VS-1, PULSE GENERATOR is an FDA 510(k)-cleared medical device (K860922) manufactured by Biotronik Sales, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 3, 1986. Regulation: 8.