# K042602: Revolution XR/D Digital Radiographic Imaging System with Manual Image Pasting

- Pathway: 510(k) (Special)
- Applicant: Ge Medical Systems, LLC
- Decided: Jan 13, 2005 after 111 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: 4 generations back to K862120 (1986). 5 ancestors in all.
8 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012389: Revolution XR/D Digital Radiographic Imaging System, Ge Medical Systems, Inc. (2001) Summary page 1.

## Most influential descendants
- K050704: Modification to:  Revolution XR/D Digital Radiographic Imaging System with Image Pasting and Autopositioning (2005), 7 descendants of its own
- K143270: Optima XR646 (2015), 6 descendants of its own
- K172869: Discovery XR656 HD (2017), 5 descendants of its own
- K231892: Definium Pace Select (2023), 1 descendant of its own
- K191699: Discovery XR656 HD with VolumeRad (2019), 1 descendant of its own

## Indications for use
Image Pasting Application for Revolution XR/d Digital Radiographic Imaging System is indicated for use in generating radiographic images of human anatomy. This device is not intended for mammographic applications.

Source page: https://510kreport.com/device/K042602
Methodology: https://510kreport.com/methodology