# K083249: Quickie Rhythm

- Pathway: 510(k) (Special)
- Applicant: Sunrise Medical Hhg, Inc.
- Decided: Dec 23, 2008 after 49 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
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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142457: Quickie, Zippie (2014), 4 descendants of its own
- K231315: Velox Power Chair (2024), 0 descendants of its own
- K213090: Frontier Series Power Wheelchairs (2021), 0 descendants of its own
- K203083: Magic 360 Power Wheelchair (2021), 0 descendants of its own
- K160031: Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models BC, SC) (2016), 0 descendants of its own

## Indications for use
The Sunrise Medical Quickie Rhythm Powered Wheelchairs intended use is to provide mobility to persons limited to a seating position that have the capability of operating a powered wheelchair. The Quickie Rhythm Power Wheelchairs provide an optional means of mobility for physically challenged people.

Source page: https://510kreport.com/device/K083249
Methodology: https://510kreport.com/methodology