# K850536: Quickie Wheelchairs

- Pathway: 510(k) (Traditional)
- Applicant: Motion Designs, Inc.
- Decided: May 2, 1985 after 80 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.
13 later devices descend from it; 4 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K120628: HELIO (2012), 4 descendants of its own
- K062660: Catalysy (2006), 4 descendants of its own
- K161425: APEX Manual Wheelchair (2016), 3 descendants of its own
- K113713: Gen_2 Mechanical Wheelchair (2012), 3 descendants of its own
- K141691: GEN_3 (2014), 2 descendants of its own

Source page: https://510kreport.com/device/K850536
Methodology: https://510kreport.com/methodology