SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9

SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9 is an FDA 510(k)-cleared medical device (K892005) 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 19, 1989. Regulation: 8.