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: DKX FDA class 2

Thin Layer Chromatography, Barbiturate

Clinical Toxicology

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The Thin Layer Chromatography system for Barbiturate is a laboratory analytical device used to separate and identify barbiturate compounds in biological samples for clinical toxicology testing. It is a Class 2 device, carrying moderate risk and requiring a 510(k) premarket notification before it can be marketed. The product code is DKX, regulated under 21 CFR 862.3150, within the Clinical Toxicology specialty. This product is eligible for third-party 510(k) review.

510(k) Clearances

2 matches
K Number
Device Name
RAPID BARBITURATE TEST STRIP AND TEST CARD, MODELS 7015 AND 7016
ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202

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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