K243685
- 510(k) number
- K243685
- Device name
- MammoScreen BD
- Applicant
- Therapixel FR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-08-22
- Date received
- 2024-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243685.pdf
Official FDA record: K243685
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.