KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP

KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP is an FDA 510(k)-cleared medical device (K902193) manufactured by Kevtek Medical Products, 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 March 14, 1991. Regulation: 8.