MODELS 5976/5977 PACEMAKER PULSE GENER

MODELS 5976/5977 PACEMAKER PULSE GENER is an FDA 510(k)-cleared medical device (K810677) manufactured by Medtronic, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 26, 1981. Regulation: 8.