RadiForce MX247W— 510(k) K262783
Substantially EquivalentEizo Corporation
FDA 510(k) clearance K262783 for RadiForce MX247W, Substantially Equivalent on 2026-09-01. Applicant: Eizo Corporation. Device class: 2.
Summary
RadiForce MX247W is from Eizo Corporation, filed under product code PGY (Display, Diagnostic Radiology). The record gives the model name and nothing else about the display.
Class II, 21 CFR 892.2050. Radiology is both the classification panel and the review panel, and it came in as an Abbreviated 510(k). The decision was Substantially Equivalent.
Eizo filed from Hakusan, Ishikawa, Japan. The decision came 26 calendar days after FDA received it (August 6 to September 1, 2026).
Clearance details
- Applicant
- Eizo Corporation
- Product code
- Product 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, Ishikawa, JP
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