# K212092: Portable Folding Electric Wheelchair (Model: DC01)

- Pathway: 510(k) (Traditional)
- Applicant: Anhui Jbh Medical Apparatus Co., Ltd.
- Decided: May 6, 2022 after 304 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: 4 generations back to K023148 (2003). 4 ancestors in all.
5 later devices descend from it; 4 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113463: Power Wheelchair, Suzhou KD Medical Appliance Co., Ltd. (2012) Summary page 4.

## Most influential descendants
- K242448: Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36) (2025), 1 descendant of its own
- K251606: Power Wheelchair (D26) (2025), 0 descendants of its own
- K241641: Electric Wheelchair (YE200) (2025), 0 descendants of its own
- K242468: Power Wheelchair (D10, D12, D15, D17, D20, D37) (2024), 0 descendants of its own
- K242252: Power Wheelchair (2024), 0 descendants of its own

## Indications for use
The wheelchair (Model: DC01) is a motor driven, indoor and outdoor transportation vehicle with the intended use to provide mobility to a disabled or elderly person limited to a seated position.

Source page: https://510kreport.com/device/K212092
Methodology: https://510kreport.com/methodology