K243221
- 510(k) number
- K243221
- Device name
- RadiForce RX570; RadiForce RX570-AR
- Applicant
- Eizo Corporation JP
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2024-11-27
- Date received
- 2024-10-07
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K243221.pdf
Official FDA record: K243221
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.