# K082288: Haida HD21

- Pathway: 510(k) (Traditional)
- Applicant: Jiangyin East China Medical Technology Co., Ltd.
- Decided: Aug 19, 2008 after 8 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: 3 generations back to K023148 (2003). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062888: Middle Wheel Drive Power Chair, CWD01, Emg Technology Co., Ltd. (2006) Summary page 1.
- K072027: Foru KV10HB, Kwang Yang Motor Co., Ltd. (2007) Summary page 1.

## Indications for use
It is a motor driven, indoor and outdoor transportation vehicles with the intended use to provide mobility to disabled or elderly persons limited to a seated position.

Source page: https://510kreport.com/device/K082288
Methodology: https://510kreport.com/methodology