Clearance Summary
XVI R5.0 received FDA 510(k) clearance under submission number K131965, sponsored by Elekta 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 2013-09-25.
- Submission: K131965
- Applicant / Sponsor: Elekta Limited
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 2013-09-25
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.