NUFFIELD ANESTHESIA VENTILATOR SER. 400

NUFFIELD ANESTHESIA VENTILATOR SER. 400 is an FDA 510(k)-cleared medical device (K803052) manufactured by Penlon, 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 January 6, 1981. Regulation: 8.