RadiForce RX570; RadiForce RX570-AR— 510(k) K243221
Substantially EquivalentEizo Corporation
FDA 510(k) clearance K243221 for RadiForce RX570; RadiForce RX570-AR, Substantially Equivalent on 2024-11-27. Applicant: Eizo Corporation. Device class: 2.
Clearance details
- Applicant
- Eizo Corporation
- Product code
- Code PGY
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Hakusan, JP
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