MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE

MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE is an FDA 510(k)-cleared medical device (K072420) manufactured by Oceanic Medical Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 2008. Regulation: 8.