SIGMA MP MULTIPLACE HYPERBARIC CHAMBER

SIGMA MP MULTIPLACE HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K930748) manufactured by Perry Baromedical Services. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 19, 1993. Regulation: 8.