SIGMA PLUS MONOPLACE HYPERBARIC CHAMBER

SIGMA PLUS MONOPLACE HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K974868) manufactured by Perry Baromedical Corp.. 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 1, 1998. Regulation: 8.