K251410
- 510(k) number
- K251410
- Device name
- VXvue
- Applicant
- Vieworks Co., Ltd. KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-11-04
- Date received
- 2025-05-07
- 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: K251410.pdf
Official FDA record: K251410
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.