# K190368: Enhanced Feature Software Pack CXDI Series

- Pathway: 510(k) (Special)
- Applicant: Canon, Inc.
- Decided: Mar 13, 2019 after 26 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: 12 generations back to K981556 (1998). 49 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 51 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153312: Scatter Correction for Cxdi Series, Canon, Inc. (2016) Summary page 4.
- K170332: Digital Radiography Cxdi-710C Wireless, Digital Radiography Cxdi-810C Wireless, Canon, Inc. (2017) Summary page 4.
- K171270: Digital Radiography Cxdi-410C Wireless, Canon, Inc. (2017) Summary page 4.

## Most influential descendants
- K212269: Intelligent NR (2021), 0 descendants of its own

## Indications for use
As a part of the CXDI series radiography system, the CXDI Control Software when used with a compatible CXDI detector is intended to provide digital image capture, processing, and display for conventional film/screen radiographic examinations. This device is intended to replace radiographic film/screen systems in all general purpose diagnostic procedures including specialist areas like intensive care, trauma, and pediatric work. This device is not intended for fluoroscopic, angiographic, or mammography applications.

Source page: https://510kreport.com/device/K190368
Methodology: https://510kreport.com/methodology