K241441
- 510(k) number
- K241441
- Device name
- RadiForce RX670; RadiForce RX670-AR
- Applicant
- Eizo Corporation JP
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2024-07-16
- Date received
- 2024-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241441.pdf
Official FDA record: K241441
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.