LIFEPAK 300 AUTOMATIC ADVISORY DEFRILLATOR

LIFEPAK 300 AUTOMATIC ADVISORY DEFRILLATOR is an FDA 510(k)-cleared medical device (K925936) manufactured by Physio-Control Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 7, 1994. Regulation: 8.