K241879
- 510(k) number
- K241879
- Device name
- vRad Viewer
- Applicant
- Virtual Radiologic Corporation MN · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-07-18
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241879.pdf
Official FDA record: K241879
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.