Cleared Traditional

K030760 - COACH 888W

K030760 is an FDA 510(k) clearance for COACH 888W, manufactured by Wheelchair & Scooter Express. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Traditional 510(k) pathway after a 121-day FDA review.

K030760 · Wheelchair & Scooter Express · Physical Medicine device
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Jul 2003
Decision
121d
Days
Class 2
Risk

K030760 is an FDA 510(k) clearance for the COACH 888W. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Wheelchair & Scooter Express (Houston, US). The FDA issued a Cleared decision on July 10, 2003 after a review of 121 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3860 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K030760

510(k) Number K030760 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 2003
Decision Date July 10, 2003
Days to Decision 121 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
5d slower than avg
Panel avg: 116d · This submission: 121d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 589
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K030760.
K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT
K033263 · Track Corporation · Oct 2003
F-10 FOLDING POWER CHAIR
K032441 · Wheelchair & Scooter Express · Oct 2003
F-11 FOLDING POWER CHAIR
K032440 · Wheelchair & Scooter Express · Sep 2003
JASON MARINE ALL TERRAIN ELECTRIC WHEELCHAIR, MODEL SEEKER II
K031342 · Jason Marine Enterprises, Inc. · Jul 2003
COMFORT POWERED WHEELCHAIR, CONQUEROR LY-EB 202
K030355 · Comfort Orthopedic Co., Ltd. · May 2003
COMFORT POWERED WHEELCHAIR, TRAVELLER LY-EB 103
K030356 · Comfort Orthopedic Co., Ltd. · May 2003
K030760 · COACH 888W
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