Medical Device Manufacturer · US , Sunnyvale , CA

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

4 submissions · 4 cleared · Since 2000

Total

Cleared

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.

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

4 devices

1-4 of 4