Medical Device Manufacturer · US , Goleta , CA

Inogen, Inc.

4 submissions · 4 cleared · Since 2004
4
Total
4
Cleared
0
Denied

Inogen, Inc. — FDA 510(k) Submissions

Inogen, Inc. has submitted 4 FDA 510(k) premarket notifications since 2004, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Generator, Oxygen, Portable, Intra-pulmonary Percussive Vibration (ipv) Devices . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Anesthesiology 4