# K060531: Quickie Rhythm & Groove Series Power Wheelchairs W/Quickie Delphi Controls

- Pathway: 510(k) (Special)
- Applicant: Sunrise Medical
- Decided: Mar 17, 2006 after 17 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Jan 11, 2008 · Not classified · Z-1532-2008: Product experiences a longer than expected stopping distance, which may cause injury to the user, objects, or the chair itself.
- Jan 11, 2008 · Not classified · Z-1531-2008: Product experiences a longer than expected stopping distance, which may cause injury to the user, objects, or the chair itself.
- Apr 23, 2007 · Not classified · Z-1163-2007: The wire harness connected to the display housing (Quickie IQ Enhanced Displays) may separate and cause sparks from a short circuit.
- Nov 13, 2006 · Not classified · Z-2339-2008: Rear bolts holding the frame in place may shear and the front bolts may potentially come off the posts, resulting in partial or full seat detachment in a sudden stop or crash.

## Indications for use
The Quickie Rhythm & Groove Series Power Wheelchairs with Quickie/Delphi Controls intended use is to empower physically challenged individuals by providing a means of mobility.

Source page: https://510kreport.com/device/K060531
Methodology: https://510kreport.com/methodology