EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF

EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF is an FDA 510(k)-cleared medical device (K914743) manufactured by Pertrach. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 9, 1992. Regulation: 8.