# K042444: Litestream 500E

- Pathway: 510(k) (Traditional)
- Applicant: Pride Mobility Products Corp.
- Decided: Oct 21, 2004 after 42 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- 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 K850536 (1985). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K850536: Quickie Wheelchairs, Motion Designs, Inc. (1985) Summary page 4.

## Most influential descendants
- K111739: Kids Rock 3 Chair (2011), 0 descendants of its own

## Indications for use
The intended use of the Litestream 500E is to provide mobility to persons limited to a seated position that are capable of operating a mechanical wheelchair. The Litestream 500E mechanical wheelchair enhances the mobility of users whom are partially or fully non-ambulatory.

Source page: https://510kreport.com/device/K042444
Methodology: https://510kreport.com/methodology