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Hyperbaric Technologies, Inc.
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OXYHEAL 2000 HYPERBARIC CHAMBER SERIES, MODEL OXYHEAL 2000 SERIES is an FDA 510(k)-cleared medical device (K011866) manufactured by Hyperbaric Technologies, 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 June 5, 2002. Regulation: 8.