# K142457: Quickie, Zippie

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical (Us), LLC
- Decided: Dec 18, 2014 after 107 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K062701 (2006). 2 ancestors in all.
4 later devices descend from it; 4 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062701: Quickie Rhapsody, MWD Series II Power Wheelchair, Sunrise Medical, Inc. (2006) Summary page 4.
- K083249: Quickie Rhythm, Sunrise Medical Hhg, Inc. (2008) Summary page 4.

## Most influential descendants
- 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

## Recalls of this device
- Feb 13, 2020 · Class II · Z-1947-2020: Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.

## Indications for use
Quickie® and Zippie® power wheelchairs are battery-operated devices with wheels that are intended for medical purposes to provide mobility to persons restricted to a sitting position. The Zippie® power wheelchairs are specifically for people who are slightly smaller in stature—including children.

Source page: https://510kreport.com/device/K142457
Methodology: https://510kreport.com/methodology