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: PCH FDA class 2

Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

Microbiology

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The Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System is a qualitative in vitro diagnostic device intended to simultaneously detect and identify multiple gastrointestinal pathogens (bacterial, viral, and parasitic) from stool specimens. It falls under the Microbiology medical specialty and is classified as a Class 2 device under regulation 866.3990, requiring 510(k) premarket notification. These multiplex panels enable rapid, comprehensive diagnosis of gastrointestinal infections in a single test. It is not an implant and is not life-sustaining.

510(k) Clearances

32 matches
K Number
Device Name
QIAstat-Dx GI Panel 2 Mini B
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel Mid
BioCode Gastrointestinal Pathogen Panel (GPP)
QIAstat-Dx GI Panel 2 Mini B&V
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
QIAstat-Dx Gastrointestinal Panel 2
EasyScreen Gastrointestinal Parasite Detection Kit
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
BD MAX Enteric Viral Panel
BD MAX Enteric Parasite Panel
xTAG Gastrointestinal Pathogen Panel (GPP)
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
EntericBio Dx Assay
Biocode Gastrointestinal Pathogen Panel (GPP)
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
BD MAX Enteric Viral Panel, BD MAX Instrument
BioCode Gastrointestinal Pathogen Panel (GPP)
BD MAX Extended Enteric Bacterial Panel, BD MAX System
FilmArray Gastrointestinal Panel (GI) for use with FilmArray Torch
Great Basin Shiga Toxin Direct Test
BD MAX Enteric Parasite Panel, BD MAX Instrument
FilmArray Gastrointestinal (GI) Panel for use with the FilmArray 2.0
Xpert Norovirus, GeneXpert Dx Systems (GX-I, GX-11, GX-IV, GX-XVI), GeneXpert Infinity-48 System, GeneXpert Infinity-48s System, GeneXpert Infinity-80 System
XTAG GASTROINTESTINAL PATHOGEN PANEL(GPP)/XTAG DATA ANALYSIS SOFTWARE FOR GPP(TDAS GPP)
VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST (EP)
XTAG GASTROINTESTINAL PATHOGEN PANEL (GPP)/XTAG DATA ANALYSIS SOFTWARE FOR GPP (TDAS GPP)
VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST ( EP)
FILMARRAY GASTROINTESTINAL (GI) PANEL
XTAG GASTROINTESTINAL PATHOGEN PANEL(GPP) XTAG DATA ANALYSIS SOFTWARE FOR GPP (TDAS GPP) LUMINEX MAGPIX
PROGASTRO SSCS ASSAY
XTAG GASTROINTESTINAL PATHOGEN PANEL (GPP) XTAG DATA ANALYSIS SOFTWARE FOR GPP (TDAS)

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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