EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K962389) manufactured by Unomedical Sdn Bhd. 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 20, 1996. Regulation: 8.