ACKRAD ENDOTRACHEAL TUBE INTRODUCING GUIDE

ACKRAD ENDOTRACHEAL TUBE INTRODUCING GUIDE is an FDA 510(k)-cleared medical device (K844557) manufactured by Ackrad Laboratories. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 16, 1984. Regulation: 8.