LINDE MARK II OXYGEN RESERV. TYPE OR-4

LINDE MARK II OXYGEN RESERV. TYPE OR-4 is an FDA 510(k)-cleared medical device (K810732) manufactured by Union Carbide 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 March 26, 1981. Regulation: 8.