ILM ENDOTRACHEAL TUBE

ILM ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K991580) manufactured by The Laryngeal Mask Co., Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 2000. Regulation: 8.