# K102110: 24 Widen Wheelchair (JY/CT-H28), 18 Reclining Wheelchair (JY-260), 18 Light Weight Wheelchair (JY/CT-H06), 18 Alumin

- Pathway: 510(k) (Traditional)
- Applicant: Foshan Shunde Jaeyong Hardware Co., Ltd.
- Decided: Oct 26, 2010 after 90 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.
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 Mechanical Wheelchairs are intended to provide mobility to persons restricted to a sitting position.

Source page: https://510kreport.com/device/K102110
Methodology: https://510kreport.com/methodology