# K041542: CT-C3000DUAL and CT-C2800DUAL Family of Dual-Slice CT Scanner Systems

- Pathway: 510(k) (Traditional)
- Applicant: Neusoft Digital Medical Systems Co., Ltd.
- Decided: Jun 17, 2004 after 9 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: 1 generation back to K020913 (2002). 1 ancestor in all.
3 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020913: CT-C3000 Spiral CT Scanner System, Neusoft Digital Medical Systems Co., Ltd. (2002) Summary page 2.

## Most influential descendants
- K062451: Neuviz Dual Multi-Slice CT Scanner System (2006), 2 descendants of its own
- K071308: Modification to Neuviz Dual Multi-Slice CT Scanner System (2007), 1 descendant of its own
- K080540: Neusoft Spiral CT Scanner System, Model Neuviz Version 2.0 (2008), 0 descendants of its own

## Indications for use
The CT-C3000DUAL and CT-C2800DUAL Family of Dual-slice CT Scanner Systems are intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data taken at different angles.

Source page: https://510kreport.com/device/K041542
Methodology: https://510kreport.com/methodology