Medical Device Manufacturer · US , Sunnyvale , CA

Aerogen, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000

Recent clearances: AERONEB II, MODEL APN 200

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aerogen, Inc. Anesthesiology ✕

4 devices

1-4 of 4

Cleared Nov 21, 2003

AERONEB GO NEBULIZER, MODEL AG-AG2000

Anesthesiology · 70d

Cleared May 15, 2002

AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000

Anesthesiology · 33d

Cleared Oct 13, 2000

AERONEB PORTABLE NEBULIZER

Anesthesiology · 15d

Cleared Aug 25, 2000

AERONEB II, MODEL APN 200

Anesthesiology · 368d