
Hypertec, Inc.
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MODEL 5000 MULTIPLACE HYPERBARIC THERAPY is an FDA 510(k)-cleared medical device (K002794) manufactured by Hypertec, 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 December 5, 2000. Regulation: 8.