LIFEPAK 1000 DEFIBRILLATOR

LIFEPAK 1000 DEFIBRILLATOR is an FDA 510(k)-cleared medical device (K122600) manufactured by Physio-Control, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on October 10, 2012. Regulation: 8.