K252332
- 510(k) number
- K252332
- Device name
- Folliscan
- Applicant
- Mim Fertility PL
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-04-20
- Date received
- 2025-07-25
- 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: K252332.pdf
Official FDA record: K252332
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.