BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500

BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500 is an FDA 510(k)-cleared medical device (K141795) manufactured by R & D Batteries, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 7, 2014. Regulation: 8.