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: DKJ FDA class 2

Colorimetry, Salicylate

Clinical Toxicology

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The Colorimetric Salicylate test uses colorimetric chemical reactions to detect and quantify salicylate compounds, including aspirin and its metabolites, in patient specimens, supporting therapeutic drug monitoring and toxicology evaluations for salicylate overdose. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is regulated under 21 CFR 862.3830 within the Clinical Toxicology specialty. The device is eligible for third-party 510(k) review.

510(k) Clearances

29 matches
K Number
Device Name
ADVIA CHEMISTRY SALICYLATE REAGENT
SALICYLATE-SL ASSAY
SALICYLATE ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
SYNCHRON SYSTEMS SALICYLATE REAGENT AND CALIBRATOR
EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109UL
SALICYLATE-SL ASSAY CATALOGUE NUMBER 511-20,511-40
SALICYLATE ASSAY (ACE), CATALOGUE NUMBER 501-71
PARAMAX SALICYLATE REAGENT
SALICYLATE ASSAY
AXSYM SALICYLATE
ABUSCREEN ONLINE(R) CALIBRATORS
DU PONT DIMENSION(R) SALICYLATE(SAL) METHOD
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (SALI)
GDS ENZYMATIC SALICYLATE REAGENT
EASY-TEST SALICYLATE (SAL) #16691
EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93
EMDS SALICYLATE (SAL) TESTPACKS, ITEM NO. 67694/95
SALICYLATE ASSAY KIT, CATALOGUE NUMBER 501-71
SALICYLATE REAGENT SET
GGTP REAGENT/SERUM IRON/SALICYLATE DEMAND ANALYZER
TDX SALICYLATE
SALICYLATE ASSAY KIT
SALICYLATE TEST
DETERMIN. OF SALICYLATE IN SERUM/PLAST
PARAMAX SALICYLATE REAGENT
SALICYLATE ASSAY KIT
TOXI-LAB RAPID SCREEN
SALICYLATES
SALICYLATE STAT-PAK

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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