PERCUTANEOUS TRACHEOSTOMY TUBE KIT

PERCUTANEOUS TRACHEOSTOMY TUBE KIT is an FDA 510(k)-cleared medical device (K931611) manufactured by Crandall Medical Devices. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1993. Regulation: 8.