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: DKC FDA class 1

Alcohol Control Materials

Clinical Toxicology

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The Alcohol Control Materials are reference specimens containing known ethanol concentrations used to validate and verify the performance of alcohol testing methods in clinical toxicology and forensic laboratories. This device is classified as FDA Class 1, indicating low risk, and is subject only to general controls without premarket notification requirements. It is regulated under 21 CFR 862.3280 within the Clinical Toxicology specialty.

510(k) Clearances

11 matches
K Number
Device Name
MAS TOX AMMONIA CONTROLLIQUID ASSAYED TOX AMMONIA CONTROL
QUALITY CONTROL MATERIAL (ASSAYED)
AMMONIA/ETHANOL CONTROLS, HIGH/LOW, CAT.# A7937/7812
BECKMAN CX AMMONIA/ALCOHOL CONTROL
ETHANOL CONTROLS, URINE, LEVELS 1,II, AND III
SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3
WHOLE BLOOD ALCOHOL CONTROL, LEVEL 1 & 2
ETHANOL CONTROLS LOW & HIGH E5133/E5258
TOXI CHEM SERUM ALCOHOL CONTROL
EMIT-ST ETHYL ALCOHOL SERUM CONTROLS
EMIT-STM ETHYL ALCOHOL URINE CONTROLS

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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