# K021075: Mechanical Daily Use Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: First World Services, Inc.
- Decided: Jul 12, 2002 after 101 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K200135: RGK Daily Range Wheelchairs (2020), 0 descendants of its own

## Indications for use
The device is a mechanical wheelchair with wheels that are turned manually and allows mobility to physically handicapped persons restricted to a sitting position and capable of manually causing the wheels to turn.

Source page: https://510kreport.com/device/K021075
Methodology: https://510kreport.com/methodology