K232045
- 510(k) number
- K232045
- Device name
- MeVis Liver Suite
- Applicant
- MeVis Medical Solutions AG DE
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2023-10-27
- Date received
- 2023-07-10
- 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: K232045.pdf
Official FDA record: K232045
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.