ENDOFLEX TRACHEAL TUBE

ENDOFLEX TRACHEAL TUBE is an FDA 510(k)-cleared medical device (K031794) manufactured by Merlyn Associates, 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 11, 2004. Regulation: 8.