# K231315: Velox Power Chair

- Pathway: 510(k) (Traditional)
- Applicant: Velox Manufacturing, Inc.
- Decided: Jan 12, 2024 after 252 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: 2 generations back to K062701 (2006). 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)
- K142457: Quickie, Zippie, Sunrise Medical (Us), LLC (2014) Summary page 5.

## Indications for use
The Velox power wheelchair is a battery operated device that is intended to provide mobility to individuals who lack mobility and who have the capability to operate a power wheelchair while being restricted to the seated position.

Source page: https://510kreport.com/device/K231315
Methodology: https://510kreport.com/methodology