# K230684: RadiForce MX217

- Pathway: 510(k) (Abbreviated)
- Applicant: Eizo Corporation
- Decided: May 12, 2023 after 60 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: 3 generations back to K092613 (2010). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190153: RadiForce MX216, Eizo Corporation (2019) Summary page 4.

## Most influential descendants
- K252780: LCD Monitor (CL1902A, CL2103F) (2025), 0 descendants of its own

## 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/K230684
Methodology: https://510kreport.com/methodology