# K915533: Quickie Carbon Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical Quickie Designs, Inc.
- Decided: Jan 22, 1992 after 43 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K120628: HELIO (2012), 4 descendants of its own
- K161425: APEX Manual Wheelchair (2016), 3 descendants of its own
- K243111: Bowhead ERA Wheelchairs (2025), 1 descendant of its own
- K260295: Helio Kids; Apex P (2026), 0 descendants of its own
- K260121: Manual Wheelchair (7101L, 7102LHD) (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K915533
Methodology: https://510kreport.com/methodology