WIRE REINFORCED ENDOTRACHEAL TUBE

WIRE REINFORCED ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K932647) manufactured by Vitaid, 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 November 1, 1993. Regulation: 8.