AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000

AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000 is an FDA 510(k)-cleared medical device (K021175) 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 May 14, 2002. Regulation: 8.