MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM

MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM is an FDA 510(k)-cleared medical device (K874663) manufactured by Ametek/Thermox Instruments Division. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 30, 1988. Regulation: 8.