SIGMA II - DUAL PLACE HYPERBARIC CHAMBER

SIGMA II - DUAL PLACE HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K862198) 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 November 11, 1986. Regulation: 8.