Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: ING FDA class 2

Elevator, Wheelchair, Portable

Physical Medicine

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A Portable Wheelchair Elevator is a motorized, non-permanently mounted lift device intended to move a person with impaired mobility, with or without a wheelchair, from one level to another. Examples include portable platform lifts and attendant-operated stair climbing devices for wheelchairs. It is classified as FDA Class 2, representing moderate risk, meaning it requires a 510(k) premarket notification demonstrating substantial equivalence to a predicate device before marketing. The product code is ING, regulated under 21 CFR 890.3930, within the Physical Medicine medical specialty. This device is eligible for third party review, meaning the 510(k) submission may be reviewed by an FDA-accredited third party organization.

510(k) Clearances

29 matches
K Number
Device Name
RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTS
LIFTKAR PT
JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT
RPL/CPL VERTICAL PLATFORM LIFTS
JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)
MERITS E700 PORCE LIFT
BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100
GENESIS VERTICAL PLATFORM LIFT
THE MULTILIFT
GARAVENTA SUPER-TRAC TRE-52
VERTICAL LIFT
STAIR-LIFT
TRUS<T>LIFT PORCH LIFT
WHEELCHAIR ELEVATOR
V-1504 VERTICAL PLATFORM LIFT
VANGATOR II
ASCENDA
WHEEL-O-VATOR
SCALAMOBIL
ULTRAGATER WHEELCHAIR LIFT
M.D.C. PORTA-LIFT
GRAVITY DOWN WHEELCHAIR LIFT
AIR CUSHIONED AUTO WHEELCHAIR LIFT ACL-200/AG-Z2
SUPERARM 2000 LIFT
WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)
HANDI PORCH ELEVATOR
HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT
HANDI-LIFT/VICTORY WHEELCHAIR LIFT
MOBILIZATION & TRACTION TABLE

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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