K233620
- 510(k) number
- K233620
- Device name
- MIM - Centiloid Scaling
- Applicant
- Mim Software, Inc. OH · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-05-20
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K233620.pdf
Official FDA record: K233620
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.