LIFEPAK 9 DEFIBRILLATOR/MONITOR

LIFEPAK 9 DEFIBRILLATOR/MONITOR is an FDA 510(k)-cleared medical device (K935674) 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 December 15, 1993. Regulation: 8.