PANTRIDGE MK III DEFIBRILLATOR/MONITOR

PANTRIDGE MK III DEFIBRILLATOR/MONITOR is an FDA 510(k)-cleared medical device (K780416) manufactured by Ipco 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 April 20, 1978. Regulation: 8.