510(k) K213526
K213526 is an FDA 510(k) premarket notification submitted by Magnettx Oncology Solutions , Ltd. for the device "Aurora-RT". The FDA issued a decision of Substantially Equivalent on May 4, 2022. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 4, 2022
- Date Received
- Nov 4, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accelerator, Linear, Medical
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type
- 510(k)