AMT ENDOTRACHEAL TUBE BRIDLE RETENTION SYSTEM

AMT ENDOTRACHEAL TUBE BRIDLE RETENTION SYSTEM is an FDA 510(k)-cleared medical device (K140097) manufactured by Applied Medical Technology, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 23, 2014. Regulation: 8.