AMSINO ENDOTRACHEAL TUBE

AMSINO ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K050785) manufactured by Amsino International, 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 July 14, 2005. Regulation: 8.