# K992066: Revolution TX/I Digital Radiographic Table System

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Aug 30, 1999 after 73 days
- Product code: KPR (System, X-Ray, Stationary)
- 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: 2 generations back to K862120 (1986). 3 ancestors in all.
104 later devices descend from it; 1 cites it directly.
0 of 108 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982196: Digital Radiographic Imaging System, GE Medical Systems (1998) Summary page 1.
- K884930: Compax Model 40, 400, 400T, General Electric Co. (1988) Summary page 2.

## Most influential descendants
- K012389: Revolution XR/D Digital Radiographic Imaging System (2001), 103 descendants of its own
- K123098: Xgeo GC80 (2013), 48 descendants of its own
- K013481: Dual Energy and Tissue Equalization Software Option (2001), 45 descendants of its own
- K140334: Xgeo GC80 (2014), 40 descendants of its own
- K150165: GC85A (2015), 36 descendants of its own

## Indications for use
The Revolution TX/i Digital Radiographic Table System is indicated for use in generating radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in all general purpose diagnostic procedures. This device is not intended for mammographic applications.

Source page: https://510kreport.com/device/K992066
Methodology: https://510kreport.com/methodology