# K071284: Model Segaego 3D Scooter

- Pathway: 510(k) (Traditional)
- Applicant: Dalton Medical Corp.
- Decided: Jul 26, 2007 after 80 days
- Product code: INI (Vehicle, Motorized 3-Wheeled)
- Device class: 2
- Regulation: 21 CFR 890.3800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The intended use of the Segaego 3D is to provide mobility to persons limited to a seated position that are capable of operating a powered scooter.

Source page: https://510kreport.com/device/K071284
Methodology: https://510kreport.com/methodology