Sheridan Endobronchial Tubes

Sheridan Endobronchial Tubes is an FDA 510(k)-cleared medical device (K180253) manufactured by Teleflex Medical. 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, 2018. Regulation: 8.