Cleared Special

K062701 - QUICKIE RHAPSODY

K062701 is an FDA 510(k) clearance for QUICKIE RHAPSODY, manufactured by Sunrise Medical, Inc.. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Special 510(k) pathway after a 14-day FDA review.

K062701 · Sunrise Medical, Inc. · Physical Medicine device
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Sep 2006
Decision
14d
Days
Class 2
Risk

K062701 is an FDA 510(k) clearance for the QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Sunrise Medical, Inc. (Longmont, US). The FDA issued a Cleared decision on September 25, 2006 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3860 - the FDA physical medicine device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Sunrise Medical, Inc. devices

FDA 510(k) Submission Details - K062701

510(k) Number K062701 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 2006
Decision Date September 25, 2006
Days to Decision 14 days
Submission Type Special
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 115d · This submission: 14d
Pathway characteristics
Modification to existing cleared device.

ITI Device Classification - Class 2, Special Controls

Product Code ITI Wheelchair, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3860
Definition 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 Of Device Is Not Intended To Climb Stairs (see Product Code: Imk).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.

Regulatory Peers - ITI Wheelchair, Powered

All 231
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K062701.
HEARTWAY ATTENDANT-CONTROLLED POWER CHAIR, TC1
K071006 · Heartway Medical Products Co., Ltd. · May 2007
WU'S POWERED WHEELCHAIR, MAMBO 36
K070655 · Wu'S Tech Co., Ltd. · Apr 2007
HEARTWAY POWER TILT SEATING SYSTEM POWER CHAIR, MODEL# P16RT
K070489 · Heartway Medical Products Co., Ltd. · Mar 2007
WU'S POWERED WHEELCHAIR, MAMBO 2
K052559 · Wu'S Tech Co., Ltd. · Sep 2005
Z-CHAIR
K052353 · Pride Mobility Products Corp. · Sep 2005
WU'S POWERED WHEELCHAIR, MAMBO 36X
K050010 · Wu'S Tech Co., Ltd. · Feb 2005