MODELS 8420 THRU 8423 PACEMAKER GENER

MODELS 8420 THRU 8423 PACEMAKER GENER is an FDA 510(k)-cleared medical device (K810734) 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 14, 1981. Regulation: 8.