MODIFIED LIFEPAK 9 MONITOR/DEFIBRILLATOR

MODIFIED LIFEPAK 9 MONITOR/DEFIBRILLATOR is an FDA 510(k)-cleared medical device (K902288) 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 February 24, 1991. Regulation: 8.