K243651
- 510(k) number
- K243651
- Device name
- VersaViewer
- Applicant
- GE Medical Systems SCS FR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-04-21
- Date received
- 2024-11-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243651.pdf
Official FDA record: K243651
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.