ENDOTRACHAEL TUBE AND HOLDER

ENDOTRACHAEL TUBE AND HOLDER is an FDA 510(k)-cleared medical device (K760998) manufactured by Mcgaw Respiratory Therapy. 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 18, 1976. Regulation: 8.