Clearance Summary
Digital C-ARM with 3D received FDA 510(k) clearance under submission number K253296, sponsored by Allengers Medical Systems Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-06-05.
- Submission: K253296
- Applicant / Sponsor: Allengers Medical Systems Limited
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 2026-06-05
Classification & Regulation
This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.