2C7153 NEBULIZER CAP

2C7153 NEBULIZER CAP is an FDA 510(k)-cleared medical device (K780406) 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 11, 1978. Regulation: 8.