K233465
- 510(k) number
- K233465
- Device name
- RadiForce MX317W
- Applicant
- Eizo Corporation JP
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2023-12-21
- Date received
- 2023-10-24
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233465.pdf
Official FDA record: K233465
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.