LIFEPAK 9 DEFIBRILLATOR & CARDIAC MONITOR/MODIFIED

LIFEPAK 9 DEFIBRILLATOR & CARDIAC MONITOR/MODIFIED is an FDA 510(k)-cleared medical device (K905510) 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 19, 1990. Regulation: 8.