K231573
- 510(k) number
- K231573
- Device name
- ThinkQA (Edition 2)
- Applicant
- Dosisoft SA FR
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2024-01-18
- Date received
- 2023-05-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K231573.pdf
Official FDA record: K231573
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.