SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER

SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER is an FDA 510(k)-cleared medical device (K100268) manufactured by Sechrist Industries, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 2010. Regulation: 8.