# K000300: Lightspeed 2.0CT Scanner System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Feb 15, 2000 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
No predicates in its family tree.
49 later devices descend from it; 4 cite it directly.
6 of 50 devices in its family (counting itself) have 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
- K051765: Ceretom, Model NL3000 (2005), 27 descendants of its own
- K052855: Starspeed Series CT Scanner Systems (2005), 17 descendants of its own
- K082816: GE Brightspeed Delight CT Scanner System (2008), 16 descendants of its own
- K093514: Discovery Model NM/CT 670 (2009), 13 descendants of its own
- K090811: Inspira HD, Model: NL1000 (2009), 10 descendants of its own

Source page: https://510kreport.com/device/K000300
Methodology: https://510kreport.com/methodology