K240705
- 510(k) number
- K240705
- Device name
- Vitrea Software Package, VSTP-002A V2.0
- Applicant
- Canon Medical Systems Corporation JP
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-07-17
- Date received
- 2024-03-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K240705.pdf
Official FDA record: K240705
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.