MODIFIED PERTRACH DISP. PEDIATRIC PERCUT. TRACHEO.

MODIFIED PERTRACH DISP. PEDIATRIC PERCUT. TRACHEO. is an FDA 510(k)-cleared medical device (K871199) 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 June 7, 1987. Regulation: 8.