K252670
- 510(k) number
- K252670
- Device name
- Alzevita
- Applicant
- TOPIA MEDTECH LIMITED GB
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-12-19
- Date received
- 2025-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252670.pdf
Official FDA record: K252670
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.