# K143101: Helio A7 Manual Wheelchair, Move Manual Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Motion Composites
- Decided: May 1, 2015 after 184 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: 1 generation back to K123975 (2013). 1 ancestor in all.
1 later device descends from it; 1 cites 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)
- K123975: Quickie & Zippie Series, Sunrise Medical (2013) Summary page 4.

## Most influential descendants
- K260295: Helio Kids; Apex P (2026), 0 descendants of its own

## Indications for use
The indications for use of the Helio A7 and Move Manual Wheelchairs is to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K143101
Methodology: https://510kreport.com/methodology