RadiForce RX670; RadiForce RX670-AR— 510(k) K241441
Substantially EquivalentEizo Corporation
FDA 510(k) clearance K241441 for RadiForce RX670; RadiForce RX670-AR, Substantially Equivalent on 2024-07-16. Applicant: Eizo Corporation.
Clearance details
- Applicant
- Eizo Corporation
- Product code
- Code PGY
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Hakusan, Ishikawa, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.