Clearance Summary
ARIETTA 50 received FDA 510(k) clearance under submission number K220295, sponsored by Fujifilm Healthcare Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2022-04-29.
- Submission: K220295
- Applicant / Sponsor: Fujifilm Healthcare Corporation
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2022-04-29
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.