# K192739: Electric Wheelchair [Models: JRWD6010/JRWD6012]

- Pathway: 510(k) (Traditional)
- Applicant: Jerry Medical Instrument (Shanghai) Co., Ltd.
- Decided: Jul 13, 2021 after 652 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- 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 K170787 (2017). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170787: Powered Wheelchair DYW30A (D09), Nanjing Jin Bai HE Medical Apparatus Co., Ltd. (2017) Summary page 5.

## Most influential descendants
- K221799: Electric Wheelchair, Model: 9000N (2022), 0 descendants of its own
- K220827: Electric Wheelchair (2022), 0 descendants of its own

## Indications for use
The device is a motor-driven, and indoor transportation vehicle with the intended use to provide mobility to a disabled or an elderly person limited to a seated position.

Source page: https://510kreport.com/device/K192739
Methodology: https://510kreport.com/methodology