# K051090: X-Change

- Pathway: 510(k) (Traditional)
- Applicant: Meyra
- Decided: May 13, 2005 after 15 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The X-Change wheelchair family is designed mostly for adults with physical impairments that require the use of a device to assist them with their mobility needs.

Source page: https://510kreport.com/device/K051090
Methodology: https://510kreport.com/methodology