TAMPA HYPERBARIC MONOPLACE CHAMBER

TAMPA HYPERBARIC MONOPLACE CHAMBER is an FDA 510(k)-cleared medical device (K981938) manufactured by Tampa Hyperbaric Ent.. 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 5, 1999. Regulation: 8.