K252937
- 510(k) number
- K252937
- Device name
- ThinkQA 3
- Applicant
- Dosisoft SA FR
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2026-06-12
- Date received
- 2025-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K252937.pdf
Official FDA record: K252937
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.