LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR

LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR is an FDA 510(k)-cleared medical device (K902478) manufactured by Physio-Control Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 1990. Regulation: 8.