# K884930: Compax Model 40, 400, 400T

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Dec 22, 1988 after 27 days
- Product code: IZZ (Table, Radiographic, Non-Tilting, Powered)
- Device class: 2
- Regulation: 21 CFR 892.1980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
293 later devices descend from it; 2 cite it directly.
0 of 294 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K971452: Multix Top/Pro Radiographic X-Ray Table (1997), 197 descendants of its own
- K983732: Thorax FD and Multix FD (1999), 187 descendants of its own
- K992066: Revolution TX/I Digital Radiographic Table System (1999), 104 descendants of its own
- K012389: Revolution XR/D Digital Radiographic Imaging System (2001), 103 descendants of its own
- K992794: Stingray DR, Model 1 (1999), 103 descendants of its own

## Recalls of this device
- Jul 30, 2009 · Not classified · Z-0457-2010: GE Healthcare has recently become aware that table lock safety features, which are provided with Compax 40E X-ray systems, are not always being utilized and has resulted in unintended lateral tabletop

Source page: https://510kreport.com/device/K884930
Methodology: https://510kreport.com/methodology