# K221799: Electric Wheelchair, Model: 9000N

- Pathway: 510(k) (Traditional)
- Applicant: Silver Fox Corporation Limited
- Decided: Sep 16, 2022 after 87 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: 2 generations back to K170787 (2017). 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)
- K192739: Electric Wheelchair [Models: JRWD6010/JRWD6012], Jerry Medical Instrument (Shanghai) Co., Ltd. (2021) Summary page 5.

## Indications for use
The Electrical Wheelchair (Model: 9000N) is a motor-driven, and indoor transportation vehicle with the intended use to provide mobility to the disabled, the elderly and the infirm for short-distance travel.

Source page: https://510kreport.com/device/K221799
Methodology: https://510kreport.com/methodology