# K062701: Quickie Rhapsody, MWD Series II Power Wheelchair

- Pathway: 510(k) (Special)
- Applicant: Sunrise Medical, Inc.
- Decided: Sep 25, 2006 after 14 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. The FDA summary names no predicate by number.

## 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 Quickie MWD Series 11 Power Wheelchair's intended use is to empower physically challenged individuals by providing a means of mobility.

Source page: https://510kreport.com/device/K062701
Methodology: https://510kreport.com/methodology