# K242989: Electric Wheelchair (MODEL H)

- Pathway: 510(k) (Traditional)
- Applicant: Nanjing E-Take Medical Apparatus Co., Ltd.
- Decided: Dec 31, 2024 after 96 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K251458: Electric Wheelchair (DH01168) (2026), 0 descendants of its own
- K250758: Electric Wheelchair (F309) (2025), 0 descendants of its own

## Indications for use
The Electric wheelchair 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/K242989
Methodology: https://510kreport.com/methodology