
Oceanic Medical Products, Inc.
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MAGELLAN-2200, MODEL 1 is an FDA 510(k)-cleared medical device (K010613) 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 October 11, 2001. Regulation: 8.