PULSE GENERATOR, LITKICRON MODEL 3-70H

PULSE GENERATOR, LITKICRON MODEL 3-70H is an FDA 510(k)-cleared medical device (K770507) manufactured by Medcor, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 6, 1977. Regulation: 8.