# K233465: RadiForce MX317W

- Pathway: 510(k) (Abbreviated)
- Applicant: Eizo Corporation
- Decided: Dec 21, 2023 after 58 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: 5 generations back to K033466 (2004). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170949: RadiForce MX315W, Eizo Corporation (2017) Summary page 4.
- K113844: Radiforce RX240, Eizo Nanao Corporation (2012) Summary page 4.

## 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/K233465
Methodology: https://510kreport.com/methodology