TRAVENOL ULTRASONIC NEBULIZER CUPS

TRAVENOL ULTRASONIC NEBULIZER CUPS is an FDA 510(k)-cleared medical device (K802054) 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 November 30, 1980. Regulation: 8.