K260234
- 510(k) number
- K260234
- Device name
- MSK Go
- Applicant
- Smart Alfa Teknoloji San. Ve Tic. A.S. TR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-05-21
- Date received
- 2026-01-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K260234.pdf
Official FDA record: K260234
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.