# K240913: Electric Wheelchair (HBLD3-B); Electric Wheelchair (HBLD3-E)

- Pathway: 510(k) (Traditional)
- Applicant: Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd
- Decided: May 31, 2024 after 58 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: 5 generations back to K023148 (2003). 5 ancestors in all.
6 later devices descend from it; 4 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220747: Power Wheelchair (N5515B), Zhejiang Innuovo Rehabilitation Devices Co.,Ltd (2022) Summary page 6.

## Most influential descendants
- K252671: Electric wheelchair (NSDS-01) (2025), 1 descendant of its own
- K242791: Electric wheelchair (KR-8807) (2024), 1 descendant of its own
- K253849: Electric wheelchair (JJW-7002, JJW-7003) (2026), 0 descendants of its own
- K251891: Electric Wheelchair (GY-E001) (2025), 0 descendants of its own
- K251285: Electric Wheelchair (HG-630) (2025), 0 descendants of its own

## Indications for use
It 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/K240913
Methodology: https://510kreport.com/methodology