# K954355: Advantage Windows 3D with Navigator Option

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Nov 14, 1995 after 57 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
758 later devices descend from it; 10 cite it directly.
1 of 759 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
- K012313: CT Colonography/NAVIGATOR2 (2001), 580 descendants of its own
- K972399: Advantage Windows Volume Rendering Option (1997), 516 descendants of its own
- K041521: Volume Viewer Plus (2004), 469 descendants of its own
- K974715: Advantage 3D XR (1998), 298 descendants of its own
- K984634: 3D-Angio (1999), 245 descendants of its own

Source page: https://510kreport.com/device/K954355
Methodology: https://510kreport.com/methodology