K241350
- 510(k) number
- K241350
- Device name
- Clarify DL
- Applicant
- Ge Medical Systems Israel, Functional Imaging IL
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-01-03
- Date received
- 2024-05-13
- 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: K241350.pdf
Official FDA record: K241350
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.