Class Class II
RadiForce RX670; RadiForce RX670-AR (K241441)
Description
RadiForce RX670; RadiForce RX670-AR by Eizo Corporation, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241441
Clearance Date2024-07-16
Clearance TypeAbbreviated
Product CodePGY
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241441
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 RX670; RadiForce RX670-AR (K241441) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K163335 | 6MP Color LCD Monitor, RadiForce RX660, RX660-AR | Eizo Corporation | 2016 |
Trace the full predicate network for K241441
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.