Cleared Special

K002616 - ELECTRIC MOBILITY RASCAL AND CHAUFFER SCOOTERS

K002616 is an FDA 510(k) clearance for ELECTRIC MOBILITY RASCAL AND CHAUFFER S..., manufactured by Electric Mobility Corp.. The device is a Class 2 Physical Medicine device with product code INI cleared through the Special 510(k) pathway after a 111-day FDA review.

K002616 · Electric Mobility Corp. · Physical Medicine device
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Dec 2000
Decision
111d
Days
Class 2
Risk

K002616 is an FDA 510(k) clearance for the ELECTRIC MOBILITY RASCAL AND CHAUFFER SCOOTERS. Classified as Vehicle, Motorized 3-wheeled (product code INI), Class II - Special Controls.

Submitted by Electric Mobility Corp. (Sewell, US). The FDA issued a Cleared decision on December 11, 2000 after a review of 111 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3800 - 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. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K002616

510(k) Number K002616 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 22, 2000
Decision Date December 11, 2000
Days to Decision 111 days
Submission Type Special
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 faster than avg
Panel avg: 116d · This submission: 111d
Pathway characteristics
Modification to existing cleared device.

INI Device Classification - Class 2, Special Controls

Product Code INI Vehicle, Motorized 3-wheeled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3800
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 Consultant

Electric Mobility, LLC
Jordan Flowers

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - INI Vehicle, Motorized 3-wheeled

All 354
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K002616 · ELECTRIC MOBILITY RASCAL AND CHAUFFER SCOOTERS
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