K242545
- 510(k) number
- K242545
- Device name
- RadiForce MX317W-PA
- Applicant
- Eizo Corporation JP
- Product code
- PZZ — Digital Pathology Display
- Decision date
- 2025-05-23
- Date received
- 2024-08-27
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242545.pdf
Official FDA record: K242545
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.