ANESTHESIA APPARATUS #FO 20S

ANESTHESIA APPARATUS #FO 20S is an FDA 510(k)-cleared medical device (K830160) manufactured by W.E. Leder Enterprises, 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 March 8, 1983. Regulation: 8.