Class Class II
RadiForce MX317W-PA (K242545)
Description
RadiForce MX317W-PA by Eizo Corporation, an FDA 510(k) cleared pathology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242545
Clearance Date2025-05-23
Clearance TypeAbbreviated
Product CodePZZ
Regulation Number864.3700
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242545
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 MX317W-PA (K242545) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K203364 | MDPC-8127 | Barco N.V. | 2021 |
Trace the full predicate network for K242545
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.