K250370
- 510(k) number
- K250370
- Device name
- SCENARIA View Phase 5.0
- Applicant
- Fujifilm Corporation JP
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2025-05-20
- Date received
- 2025-02-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K250370.pdf
Official FDA record: K250370
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.