Clearance Summary
Aurora-RT received FDA 510(k) clearance under submission number K213526, sponsored by Magnettx Oncology Solutions , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2022-05-04.
- Submission: K213526
- Applicant / Sponsor: Magnettx Oncology Solutions , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 2022-05-04
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.