K251883
- 510(k) number
- K251883
- Device name
- MIM LesionID Pro
- Applicant
- Mim Software, Inc. OH · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-12-11
- Date received
- 2025-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251883.pdf
Official FDA record: K251883
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.