HYPERBARIC OXYGEN CHAMBER

HYPERBARIC OXYGEN CHAMBER is an FDA 510(k)-cleared medical device (K790693) manufactured by Hyperbaric Oxygen Therapy, 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 July 29, 1979. Regulation: 8.