FDA cleared the RadiForce MX247W from Eizo Corporation on Sep 1, 2026 under K262783, a abbreviated 510(k). The device falls under product code PGY, Display, Diagnostic Radiology, regulated at 21 CFR 892.2050 as a Class 2 device. The review panel was Radiology.
FDA logged the submission as received on Aug 6, 2026. The decision came 26 days later, inside the 90 FDA-day goal for a 510(k).
This is the only decision on file for Eizo Corporation in the last 12 months of the tracker.
K262783 is the FDA 510(k) for RadiForce MX247W, submitted by Eizo Corporation. FDA's decision date was Sep 1, 2026, under product code PGY (Display, Diagnostic Radiology).
Eizo Corporation, based in Hakusan, Ishikawa, is the applicant of record for K262783.
FDA received the submission on Aug 6, 2026 and issued its decision on Sep 1, 2026, 26 days later.
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