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: DIH FDA class 1

Colorimetry, Cholinesterase

Clinical Toxicology

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The Colorimetric Cholinesterase test is a laboratory reagent system used to measure cholinesterase enzyme activity in blood or plasma through colorimetric methods, helping to identify toxic exposure to organophosphate compounds or to diagnose conditions causing cholinesterase deficiency. It is classified as FDA Class 1, indicating low risk, and is subject only to general controls without premarket notification. The device is regulated under 21 CFR 862.3240 within the Clinical Toxicology specialty.

510(k) Clearances

26 matches
K Number
Device Name
SYNCHRON SYSTEMS CHOLINESTERASE (CHEX) MODEL A53722
CHOLINESTERASE GEN.2 TEST SYSTEM
SENTINEL CHOLINESTERASE LIQUID
OLYMPUS CHOLINESTERASE REAGENT (CATALOG NUMBER OSR6114)
WIENER LAB COLINESTERASA AA
ADVIA 1650 CHOLINESTERASE ASSAY
CARESIDE CHOLINESTERASE
ADVIA IMS
TEST-MATE CHE CHOLINESTERASE TEST SYSTEM
IL TEST CHOLINESTERASE
CHOLINESTERASE ASSAY KIT, CATALOGUE# 300-05
IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE
KODAK EKTACHEM DT SLIDES (CHE)
CHOLINESTERASE TEST KIT
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES
BECKMAN CHOLINESTERASE REAGENT KIT
CHOLINESTERASE REAGENT, DIBUCAINE & FLUORIDE
CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
ATYPICAL CHOLINESTERASE
DU PONT DIMENSION PSEUDOCHOLINESTERASE METHOD
CHOLINESTERASE (BTC) REAGENT
CHOLINESTERASE (PTC) REAGENT
CHOLINESTERASE
RAICHEM CHOLINESTERASE REAGENT
CHOLINESTERASE REAGENT

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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