Clearance Summary
Fibresolve received FDA 510(k) clearance under submission number DEN220040, sponsored by Imvaria, Inc.. The device was reviewed via the Direct premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-01-12.
- Submission: DEN220040
- Applicant / Sponsor: Imvaria, Inc.
- Clearance pathway: Direct
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2085
- Decision date: 2024-01-12
Classification & Regulation
This clearance is catalogued under FDA product code QWO and 21 CFR 892.2085, within the Radiology review panel as a Class II device.