PERCUTANEOUS TRACHEOSTOMY DEVICE

PERCUTANEOUS TRACHEOSTOMY DEVICE is an FDA 510(k)-cleared medical device (K832498) manufactured by Frederic J. Toye, M.D.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 13, 1983. Regulation: 8.