Cleared Traditional

K024346 - THE MULTILIFT

K024346 is an FDA 510(k) clearance for THE MULTILIFT, manufactured by Services Industriels Savaria, Inc.. The device is a Class 2 Physical Medicine device with product code ING cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K024346 · Services Industriels Savaria, Inc. · Physical Medicine device
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Optimized for regulatory review, auditing and printing
Mar 2003
Decision
67d
Days
Class 2
Risk

K024346 is an FDA 510(k) clearance for the THE MULTILIFT. Classified as Elevator, Wheelchair, Portable (product code ING), Class II - Special Controls.

Submitted by Services Industriels Savaria, Inc. (Washington, US). The FDA issued a Cleared decision on March 4, 2003 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3930 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Services Industriels Savaria, Inc. devices

FDA 510(k) Submission Details - K024346

510(k) Number K024346 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 2002
Decision Date March 04, 2003
Days to Decision 67 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 115d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ING Device Classification - Class 2, Special Controls

Product Code ING Elevator, Wheelchair, Portable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3930
Definition A Motorized Lift Device That Is Not Permanently Mounted In One Location And That Is Intended For Medical Purposes To Provide A Means To Move A Person With Impaired Mobility, With Or Without A Wheelchair, From One Level To Another (e.g., Portable Platform Lifts, Attendant-operated Stair Climbing Devices For Wheelchairs).
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 - ING Elevator, Wheelchair, Portable

All 9
Devices cleared under the same product code (ING) and FDA review panel - the closest regulatory comparables to K024346.
RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTS
K113065 · Bella Elevator, LLC · Feb 2012
LIFTKAR PT
K110495 · Sano Transportgerate GmbH · May 2011
MERITS E700 PORCE LIFT
K073513 · Merits Health Products Co., Ltd. · Jan 2008
VERTICAL LIFT
K983526 · Barnes,Richardson & Colburn · Dec 1998
STAIR-LIFT
K981486 · Garaventa (Canada) , Ltd. · Jul 1998
TRUSLIFT PORCH LIFT
K964134 · Trus T Lift · Dec 1996