LIFEFORCE CLINICAL HYPERBARIC FACILITY

LIFEFORCE CLINICAL HYPERBARIC FACILITY is an FDA 510(k)-cleared medical device (K951125) manufactured by Reimers Systems, 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 1, 1995. Regulation: 8.