Cleared Traditional

K003059 - LASER 4SPSC340

K003059 is an FDA 510(k) clearance for LASER 4SPSC340, manufactured by Pride Mobility Products Corp.. The device is a Class 2 Physical Medicine device with product code INI cleared through the Traditional 510(k) pathway after a 150-day FDA review.

K003059 · Pride Mobility Products Corp. · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2001
Decision
150d
Days
Class 2
Risk

K003059 is an FDA 510(k) clearance for the LASER 4SPSC340. Classified as Vehicle, Motorized 3-wheeled (product code INI), Class II - Special Controls.

Submitted by Pride Mobility Products Corp. (Exeter, US). The FDA issued a Cleared decision on March 1, 2001 after a review of 150 days - an extended review cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3800 - 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.

View all Pride Mobility Products Corp. devices

FDA 510(k) Submission Details - K003059

510(k) Number K003059 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 2000
Decision Date March 01, 2001
Days to Decision 150 days
Submission Type Traditional
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
34d slower than avg
Panel avg: 116d · This submission: 150d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 Peers - INI Vehicle, Motorized 3-wheeled

All 318
Devices cleared under the same product code (INI) and FDA review panel - the closest regulatory comparables to K003059.
MODIFICATION TO SOLO
K011107 · Ranger All Season Corp. · May 2001
SAFARI
K010606 · Ranger All Season Corp. · Mar 2001
LASER 3 SPSC300
K003058 · Pride Mobility Products Corp. · Mar 2001
MODELS LYNX AND PANTHER MOTORIZED SCOOTERS, MODELS LYNX SX-3, LYNX SX-3P, LYNX LX-3, LYNX LX-3, PANTHER LX-4
K010135 · Invacare Corp. · Feb 2001
TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER
K003815 · Merits Health Products., Inc. · Dec 2000
ELECTRIC MOBILITY RASCAL AND CHAUFFER SCOOTERS
K002616 · Electric Mobility Corp. · Dec 2000