Cleared Special

K011993 - QUANTUM BLAST

K011993 is an FDA 510(k) clearance for QUANTUM BLAST, manufactured by Pride Mobility Products Corp.. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Special 510(k) pathway after a 17-day FDA review.

K011993 · 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
Jul 2001
Decision
17d
Days
Class 2
Risk

K011993 is an FDA 510(k) clearance for the QUANTUM BLAST. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Pride Mobility Products Corp. (Exeter, US). The FDA issued a Cleared decision on July 13, 2001 after a review of 17 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 Pride Mobility Products Corp. devices

FDA 510(k) Submission Details - K011993

510(k) Number K011993 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 26, 2001
Decision Date July 13, 2001
Days to Decision 17 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
99d faster than avg
Panel avg: 116d · This submission: 17d
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 499
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K011993.
MP-3C POWER BASE CHAIR, MODEL MP3C
K011687 · Merits Health Products., Inc. · Aug 2001
TRS-2000 POWER TILT/POWER RECLINE SYSTEM
K012281 · Accelerated Rehab Designs, Inc. · Aug 2001
SUPREMA POWERED WHEELCHAIR
K010600 · Luigi Chinetti · Jul 2001
PRAIRIE CRUISER
K002580 · Raye'S, Inc. · Jul 2001
THE NIMBLE ROCKET POWERED WHEELCHAIR
K010941 · Nimble, Inc. · Jun 2001
ALANTE, BATTERY OPERATED POWER WHEELCHAIR
K011153 · Golden Technologies, Inc. · May 2001