EUROMEDICAL POLY TRACHEOTOMY TUBE

EUROMEDICAL POLY TRACHEOTOMY TUBE is an FDA 510(k)-cleared medical device (K945874) manufactured by Regulatory & Marketing Services, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 26, 1994. Regulation: 8.