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: DML FDA class 2

Nad-Nadh, Specific Reagent For Alcohol Enzyme Method

Clinical Toxicology

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The NAD-NADH Specific Reagent for the Alcohol Enzyme Method is a laboratory reagent used in enzymatic assays that measure alcohol concentrations based on the alcohol dehydrogenase reaction, with NAD/NADH serving as the coenzyme system. It is a Class 2 device requiring a 510(k) premarket notification. The product code is DML, regulated under 21 CFR 862.3040, within the Clinical Toxicology specialty. It is eligible for third-party 510(k) review.

510(k) Clearances

13 matches
K Number
Device Name
ETHANOL
SYVA EMIT II PLUS ETHYL ALCOHOL ASSAY, MODELS 9K309UL/9K409UL
ON.SITE ALCOHOL
AXSYM REA ETHANOL
BOEHRINGER MANNHEIM ETHYL ALCOHOL ASSAY
ON*SITE ALCOHOL
SIGMA PROCEDURE NO. 333-UV
RAICHEM(TM) ALCOHOL REAGENT
KINETIC 610 ETHANOL
EMDS(TM) ALCOHOL TESTPACKS, #67691/95
PARAMAX ALCOHOL REAGENT
EMIT ST SERUM ETHYL ALCOHOL ASSAY
EMIT ST URINE ETHYL ALCOHOL ASSAY

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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