# K221876: Digital Radiography CXDI-Pro, Digital Radiography D1

- Pathway: 510(k) (Special)
- Applicant: Canon, Inc.
- Decided: Jul 15, 2022 after 17 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: 13 generations back to K981556 (1998). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220098: Digital Radiography CXDI-Pro, Digital Radiography D1, Canon, Inc. (2022) Summary page 4.

## Most influential descendants
- K222855: Digital Radiography CXDI-Pro, Digital Radiography D1 (2022), 0 descendants of its own

## Indications for use
The DIGITAL RADIOGRAPHY CXDI-Pro / D1 provides digital image capture for conventional film/screen radiographic examinations. This device is intended to capture, for display, radiographic images of human anatomy, and to replace radiographic film/screen systems in all general purpose diagnostic procedures. This device is not intended for mammography applications.

Source page: https://510kreport.com/device/K221876
Methodology: https://510kreport.com/methodology