# K262783: RadiForce MX247W

- Pathway: 510(k) (Abbreviated)
- Applicant: Eizo Corporation
- Decided: Sep 1, 2026 after 26 days
- Product code: PGY (Display, Diagnostic Radiology)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K092613 (2010). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221136: RadiForce MX243W, Eizo Corporation (2022) Summary page 5.

## Indications for use
This Product is indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.

Source page: https://510kreport.com/device/K262783
Methodology: https://510kreport.com/methodology