K243012
- 510(k) number
- K243012
- Device name
- MIM Symphony HDR Fusion
- Applicant
- Mim Software, Inc. OH · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-10-23
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K243012.pdf
Official FDA record: K243012
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.