K241300
- 510(k) number
- K241300
- Device name
- ViewPoint 6
- Applicant
- Ge Healthcare GmbH DE
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-07-02
- Date received
- 2024-05-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K241300.pdf
Official FDA record: K241300
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.