# K200135: RGK Daily Range Wheelchairs

- Pathway: 510(k) (Traditional)
- Applicant: Rgk Wheelchairs, Ltd.
- Decided: Sep 10, 2020 after 233 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 K021075 (2002). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021075: Mechanical Daily Use Wheelchair, First World Services, Inc. (2002) Summary page 4.
- K123975: Quickie & Zippie Series, Sunrise Medical (2013) Summary page 4.

## Indications for use
The RGK Daily Range Wheelchairs are mechanical wheelchairs 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/K200135
Methodology: https://510kreport.com/methodology