# K871859: CT9800 Quick 3D #B7919DA

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Aug 12, 1987 after 91 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
517 later devices descend from it; 1 cites it directly.
1 of 518 devices in its family (counting itself) has 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
- K972399: Advantage Windows Volume Rendering Option (1997), 516 descendants of its own
- K041521: Volume Viewer Plus (2004), 469 descendants of its own
- K061696: Iqqa-Liver Software (2006), 217 descendants of its own
- K063324: Pet Vcar (2007), 204 descendants of its own
- K091373: Syngo Trued (2009), 200 descendants of its own

Source page: https://510kreport.com/device/K871859
Methodology: https://510kreport.com/methodology