# K132257: Manual Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Zhejiang Jiafeng Electrical & Mechanial Co., Ltd.
- Decided: Feb 13, 2014 after 209 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- 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 K020472 (2002). 4 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062311: Karma Manual Wheelchair, Model Budget 800, Karma Medical Products Co., Ltd. (2006) Summary page 1.

## Most influential descendants
- K151797: Nuocande Plastic Manual Wheelchair Model NKD L07 (2015), 1 descendant of its own
- K180309: Manual Wheelchair W54 (2019), 0 descendants of its own

## Indications for use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position. It is designed for use indoors and outdoors, over smooth surfaces (all standard indoor flooring surfaces, concrete, asphalt and packed dirt) that are free of large obstacles and inclines greater than 8 degrees.

Source page: https://510kreport.com/device/K132257
Methodology: https://510kreport.com/methodology