# K113844: Radiforce RX240

- Pathway: 510(k) (Traditional)
- Applicant: Eizo Nanao Corporation
- Decided: Feb 27, 2012 after 61 days
- Product code: LLZ (System, Image Processing, Radiological)
- 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: 1 generation back to K092613 (2010). 1 ancestor in all.
11 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)
- K092613: Color LCD Monitor, Model Radiforce RS210, Eizo Nanao Corporation (2010) Summary page 1.

## Most influential descendants
- K150106: 2MP Color LCD Monitor, RadiForce RS240 (2015), 5 descendants of its own
- K160247: 2MP Color LCD Monitor, RadiForce RX250 and RX250-AR (2016), 4 descendants of its own
- K151861: JUSHA-C23C LCD Monitor (2015), 3 descendants of its own
- K183498: JUSHA-C270G/ JUSHA-C270/ C270G/ C270 LCD Monitor (2019), 2 descendants of its own
- K172815: 2MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+) (2017), 1 descendant of its own

## Indications for use
The RadiForce RX240 is intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The device does not support the display of mammography images for diagnosis.

Source page: https://510kreport.com/device/K113844
Methodology: https://510kreport.com/methodology