Class Class II
RadiForce GX570; RadiForce GX570-AR (K252030)
Description
RadiForce GX570; RadiForce GX570-AR by Eizo Corporation, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK252030
Clearance Date2025-08-28
Clearance TypeAbbreviated
Product CodePGY
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K252030
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. RadiForce GX570; RadiForce GX570-AR (K252030) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K181609 | RadiForce GX560, GX560-AR | Eizo Corporation | 2018 |
Trace the full predicate network for K252030
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.