# K200485: RadiForce RX1270, RadiForce RX1270-AR

- Pathway: 510(k) (Abbreviated)
- Applicant: Eizo Corporation
- Decided: Mar 23, 2020 after 25 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 K103792 (2011). 4 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172738: RadiForce RX560, RX560-AR, Eizo Corporation (2017) Summary page 4.

## Most influential descendants
- 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
- K253242: LCD Monitor (C1216W, C822W, C821W) (2025), 0 descendants of its own
- K210491: CW120N (2021), 0 descendants of its own

## Indications for use
This product is indicated for use in displaying radiological images (including full-field digital mammography and digital breast tomosynthesis) for review, analysis, and diagnosis by trained medical practitioners.

Source page: https://510kreport.com/device/K200485
Methodology: https://510kreport.com/methodology