# K192658: Manual Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Jerry Medical Instrument (Shanghai) Co., Ltd.
- Decided: Apr 1, 2020 after 189 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: 12 generations back to K020472 (2002). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180852: Manual Wheelchair, Jiangyin Newrise Medical Equipment Co., Ltd. (2019) Summary page 4.

## Indications for use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Source page: https://510kreport.com/device/K192658
Methodology: https://510kreport.com/methodology