NEBULIZER, DISP, 2D0815

NEBULIZER, DISP, 2D0815 is an FDA 510(k)-cleared medical device (K780119) 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 April 2, 1978. Regulation: 8.