# K162344: Innolux Ric

- Pathway: 510(k) (Traditional)
- Applicant: Innolux Corporation
- Decided: Dec 20, 2016 after 120 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K981556 (1998). 37 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142003: FDR D-Evo II Flat Panel Detector System, Fujifilm Medical System U.S.A., Inc. (2014) Summary page 4.
- K122865: Vivix-S Wireless, Vieworks Co., Ltd. (2013) Summary page 4.

## Most influential descendants
- K172784: DX-D Imaging Package (2017), 0 descendants of its own

## Indications for use
The Wireless/Wired INNOLUX RIC flat panel detector is intended to capture for display radiographic images of human anatomy. It is intended for use in general projection radiographic applications including pediatric and neonatal exams wherever conventional film/screen or CR systems may be used. The INNOLUX RIC is not intended for mammography, fluoroscopy, tomography, and angiography applications.

Source page: https://510kreport.com/device/K162344
Methodology: https://510kreport.com/methodology