# K172738: RadiForce RX560, RX560-AR

- Pathway: 510(k) (Traditional)
- Applicant: Eizo Corporation
- Decided: Nov 8, 2017 after 57 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 K103792 (2011). 3 ancestors in all.
11 later devices descend from it; 4 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162497: 5MP Monochrome LCD Monitor, RadiForce GX550, GX550-AR, Eizo Corporation (2016) Summary page 4.

## Most influential descendants
- K223423: 32HQ713D (2023), 3 descendants of its own
- K200485: RadiForce RX1270, RadiForce RX1270-AR (2020), 3 descendants of its own
- K230845: 32HL512D, 31HN713D, 32HQ713D (2023), 2 descendants of its own
- K231026: 12MP Color LCD Monitor C1216W, C12*** (* = 0 to 9, A to Z or blank, and the difference among models means the product is named according to different appearance colors and customer models) (2023), 1 descendant of its own
- K232127: 21HQ513D, 32HL512D, 31HN713D, 32HQ713D (2023), 1 descendant of its own

## Indications for use
This product is intended to be used in displaying and viewing digital images, including standard and multiframe digital mammography, for review, analysis and diagnosis by trained medical practitioners. It is specially designed for breast tomosynthesis applications.

Source page: https://510kreport.com/device/K172738
Methodology: https://510kreport.com/methodology