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: KHX FDA class 1

Platform, Force-Measuring

Physical Medicine

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Force-Measuring Platform is a physical medicine diagnostic device consisting of a platform instrumented with force transducers that measures ground reaction forces during standing, walking, or other activities, used to assess balance, gait biomechanics, and postural stability for rehabilitation evaluation and treatment planning. It is classified as FDA Class 1, the lowest risk category, subject to general controls only, meaning it does not require premarket notification or approval. The product code is KHX, regulated under 21 CFR 890.1575, within the Physical Medicine medical specialty.

510(k) Clearances

15 matches
K Number
Device Name
COMMUNITY BALANCE PERFORMANCE MONITOR OR COMMUNITY BPM
BALANCE MANAGER
STABILITY SYSTEM (110V) MODEL 945-300; STABILITY SYSTEM (220V) MODEL #945-302
SMS BALANCE PERFORMANCE MONITOR
FORCE MEASURING PLATFORM
COMPUTERIZED FUNCTIONAL TESTING GAIT SYSTEM
DYNAMIC SYSTEM COMPUTERIZED PODIATRIC ANALYZER
BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM
BIOMECHANICS FORCE PLATFORM/# OR6-5-1000 & 2000
BIOMECHANICS FORCE PLATFORM #LG6-4-1000 & 2000
BIOMECHANICS FORCE PLATFORM/#OR 6-6-1000 & 2000
MULTI-CHANNEL STRAIN-GAGE AMPLIFIER & POWER SUPPLY
DUAL FORCEPLATE
ELECTRODYNOGRAM SYSTEM
HEART-ALERT

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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