Aerogen, Inc. is one of 25731 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aerogen, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AERONEB GO NEBULIZER, MODEL AG-AG2000, AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000, AERONEB PORTABLE NEBULIZER
4
Total
4
Cleared
0
Denied
Aerogen, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 4 cleared submissions from 2000 to 2003. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Aerogen, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Product Service, Inc., Tuv America, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Aerogen, Inc.
4 devices
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