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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: NIJ FDA class 2

System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species

Microbiology

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The Genotypic Detection System for Resistant Markers in Enterococcus Species is an in vitro diagnostic device intended to detect the presence of the vanA and vanB genes in isolated colonies of Enterococcus spp. as a marker for vancomycin resistance, using DNA probe technology. It is classified as FDA Class 2 (Special Controls), requiring 510(k) clearance, under product code NIJ and regulation 21 CFR 866.1640 in the Microbiology specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

6 matches
K Number
Device Name
Xpert vanA
IMDX VANR FOR ABBOTT M2000
BD GENEOHM VANR ASSAY
Xpert VanA Assay
IDI-VANR ASSAY
VELOGENE GENOMIC IDENTIFICATIONASSAY FOR VRE

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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