SANDS SERIES III HYPERBARIC CHAMBER

SANDS SERIES III HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K972908) manufactured by Sands Hyperbarics. 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 21, 1998. Regulation: 8.