SINGLE USE NEBULIZER, ADJUST. AIR-

SINGLE USE NEBULIZER, ADJUST. AIR- is an FDA 510(k)-cleared medical device (K830895) manufactured by Airlife, 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 April 27, 1983. Regulation: 8.