# K033502: Lightspeed 6.0 CT Scanner System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, LLC
- Decided: Nov 20, 2003 after 15 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: 2 generations back to K013561 (2001). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030420: Lightspeed 5.0 Computed Tomography System, GE Medical Systems (2003) Summary page 1.
- (no number) Lightspeed 4.0 CT Scanner System: named in the summary without a submission number

## Most influential descendants
- K052447: Synerad Impact 60, Synerad Impact 72 and Analogic AMS1600 (2005), 0 descendants of its own

## Indications for use
The Lightspeed 6.0 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications.

Source page: https://510kreport.com/device/K033502
Methodology: https://510kreport.com/methodology