LINDE OXYGEN WALKER SYS. MARK II-L

LINDE OXYGEN WALKER SYS. MARK II-L is an FDA 510(k)-cleared medical device (K791902) 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 October 16, 1979. Regulation: 8.