MODEL 3000 HYPERBARIC CHAMBER

MODEL 3000 HYPERBARIC CHAMBER is an FDA 510(k)-cleared medical device (K841608) manufactured by Custom Craft Products, 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 May 1, 1984. Regulation: 8.