SURGITEK ENDOTRACHEAL TUBE, LASER RESIS

SURGITEK ENDOTRACHEAL TUBE, LASER RESIS is an FDA 510(k)-cleared medical device (K823757) manufactured by Medical Engineering Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 1983. Regulation: 8.