# K182591: RadiForce RX360, RX360-AR

- Pathway: 510(k) (Abbreviated)
- Applicant: Eizo Corporation
- Decided: Oct 18, 2018 after 28 days
- Product code: PGY (Display, Diagnostic Radiology)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K033466 (2004). 5 ancestors in all.
7 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153354: 3MP Color LCD Monitor, RadiForce RX350, Eizo Corporation (2016) Summary page 4.

## Most influential descendants
- K201211: 3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+ (2020), 4 descendants of its own
- K240310: LCD Monitors C310S, G310S, C316S, G316S, C616W (2024), 1 descendant of its own
- K243031: LCD Monitors C310S, G310S, C316S, G316S, C616W (2024), 0 descendants of its own
- K233336: 21.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01) (2024), 0 descendants of its own
- K223768: RadiForce RX270 (2023), 0 descendants of its own

## Recalls of this device
- Jul 30, 2019 · Class II · Z-2294-2020: Under certain conditions, a marble pattern infrequently appears on the monitor.

## 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/K182591
Methodology: https://510kreport.com/methodology