# K992884: Wheelchair (Manual, Not Electrical)

- Pathway: 510(k) (Traditional)
- Applicant: Foshan Machinery & Equipment Import & Export Co.
- Decided: Nov 2, 1999 after 69 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K041814: FS Series Wheelchair (2004), 0 descendants of its own

## Indications for use
In order to transport patient(s) and/or disable people This particular wheel chair is manual,not electrical device. It is highly recommended that someone(nurse, assistant,nursing home staff or family member) operates this device to transport patient(s) and/or disable people on even surface like concerete road,pavement and floor for the safety and effectiveness.

Source page: https://510kreport.com/device/K992884
Methodology: https://510kreport.com/methodology