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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: KNO FDA class 1

Accessories, Wheelchair

Physical Medicine

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Wheelchair Accessories are supplemental attachments, cushions, trays, bags, and other add-on items designed to enhance the comfort, function, safety, or adaptability of wheelchairs for individuals with mobility impairments. It is classified as FDA Class 1, indicating low risk subject to general controls with no premarket submission required. The product code is KNO and the applicable regulation is 21 CFR 890.3910 in the Physical Medicine specialty. This device is GMP exempt.

510(k) Clearances

35 matches
K Number
Device Name
REDMAN ACCESSORIES
VELCRO STRAPS TO HOLD ARM TO WHEELCHAIR
FRICTION FEEDER
WHEELCHAIR PATIENT RESTRAINTS
CUSHIONS FOR WHEELCHAIR ARMS
ARM THROUGH FOR WHEELCHAIR BK-6459-01 &
CLAMP ON HOLDER FOR A GLASS OR CUP
HEAD SUPPORT FOR WHEELCHAIR
WHEEL CHAIR ACCESSORIES
WHEELCHAIR PAL
BK-6453 RIMMED ACRYLIC LAP TRAY KIT
WHEELCHAIR ACCESSORIES
INCONTINENT PAD
WHEELCHAIR RAMPS
WHEELCHAIR ACCESSORIES
BODY STRAP
WHEELCHAIR ACCESSORIES
BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF
EZ ON SAFETY PONCHO
HAMILTON TUCKAWAY DESK
SKIL-CARE LEG PADS
ASHTRAY FOR WHEELCHAIR
ADJUSTABLE HEIGHT DESK ARM LAP TRAY KIT
BAG, WHEELCHAIR
TRAY, LAP, MOLDED
VEST, SUPPORT, TRUNK
BAG, WALDER
WHEELCHAIR MUFF
HEEL LOOPS
TOE LOOPS
STRAP, LEGREST
CANE OR CRUTCH PARKER (3/4, 7/8, L)
ADJUSTER, WHEELCHAIR WIDTH, BK-6470
CARPET COVERS FOR FOOTRESTS, BK-6467
DESK, BEANBAG SHUFFLE, BK-6059

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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