MODEL 3200P/3200PR HYPERBARIC CHAMBER

MODEL 3200P/3200PR HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K950386) 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 June 12, 1995. Regulation: 8.