# K142697: NExCT 7

- Pathway: 510(k) (Traditional)
- Applicant: Neurologica Corporation
- Decided: Dec 23, 2014 after 92 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
Longest line of descent: 8 generations back to K944131 (1995). 27 ancestors in all.
No later device cites it as a predicate yet.
1 of 28 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102677: Bodytom NL 4000, Neurologica Corporation (2011) Summary page 5.
- K122109: Aquilion One Vision, V4.90, Toshiba America Medical Systems, In.C (2012) Summary page 5.

## Indications for use
The NLS128 [NExCT 7] system is intended to be used for x-ray computed tomography applications that produce cross sectional images for anatomy that can be imaged in the system aperture. The NExCT 7 is intended to be used for both pediatric and adult imaging and as such has preset dose settings based upon weight and age.

Source page: https://510kreport.com/device/K142697
Methodology: https://510kreport.com/methodology