AERONEB II, MODEL APN 200

AERONEB II, MODEL APN 200 is an FDA 510(k)-cleared medical device (K992831) 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 August 24, 2000. Regulation: 8.