OHIO NON-REUSABLE TRACHEAL TUBE MURPHY

OHIO NON-REUSABLE TRACHEAL TUBE MURPHY is an FDA 510(k)-cleared medical device (K812879) manufactured by Airco/Ohio Medical Products. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 23, 1981. Regulation: 8.