NEBULIZER SET-2C7105

NEBULIZER SET-2C7105 is an FDA 510(k)-cleared medical device (K772222) manufactured by Travenol Laboratories, S.A.. 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 21, 1977. Regulation: 8.