AERONEB GO NEBULIZER, MODEL AG-AG2000

AERONEB GO NEBULIZER, MODEL AG-AG2000 is an FDA 510(k)-cleared medical device (K032849) manufactured by Aerogen, 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 November 20, 2003. Regulation: 8.