MODEL 5985 PACEMAKER PULSE GENERATOR

MODEL 5985 PACEMAKER PULSE GENERATOR is an FDA 510(k)-cleared medical device (K800285) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 19, 1980. Regulation: 8.