Clearance Summary
Inogen Rove 6 received FDA 510(k) clearance under submission number K230052, sponsored by Inogen, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2023-06-30.
- Submission: K230052
- Applicant / Sponsor: Inogen, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5440
- Decision date: 2023-06-30
Classification & Regulation
This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.