MICROTHIN-DI BIPOLAR PULSE GENERATOR

MICROTHIN-DI BIPOLAR PULSE GENERATOR is an FDA 510(k)-cleared medical device (K802409) manufactured by Cardiac Pacemakers, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on October 30, 1980. Regulation: 8.