Quickie Rhapsody, MWD Series II Power Wheelchair

FDA 510(k) K062701 · Sunrise Medical, Inc.

Substantially Equivalent

510(k) numberK062701

Submission

Device name
Quickie Rhapsody, MWD Series II Power Wheelchair
Applicant
Sunrise Medical, Inc.
Longmont, CO, US
Received
September 11, 2006
Decision date
September 25, 2006
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ITI – Wheelchair, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3860
Specialty
Physical Medicine

A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to mean the device type is intended to provide mobility to individuals who have mobility impairments and require an assistive device for mobility. NOTE: This type…

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Questions and answers

When was Quickie Rhapsody, MWD Series II Power Wheelchair cleared by the FDA?

Quickie Rhapsody, MWD Series II Power Wheelchair (K062701) received a 510(k) decision of Substantially Equivalent on September 25, 2006, 14 days after the submission was received.

What is the product code of K062701?

The FDA product code is ITI – Wheelchair, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.3860.