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: GMZ FDA class 1

Antigens, All Types, Escherichia Coli

Microbiology

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The Antigens for All Types of Escherichia Coli are serotyping reagents used in microbiology laboratories to characterize E. coli strains through antigen-based methods, aiding in the epidemiological investigation of infections and outbreaks. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls without a premarket submission requirement. The product code is GMZ, regulated under 21 CFR 866.3255 in the Microbiology specialty.

510(k) Clearances

14 matches
K Number
Device Name
Curian® Shiga Toxin
SHIGA TOXIN CHEK
SHIGA TOXIN QUIK CHEK
IMMUNOCARD STAT! EHEC, MODEL 751630
BIOSTAR OIA SHIGATOX
IMMUNOCARD STAT! E. COLI O157 PLUS
IMMUNOCARD STAT! E. COLI O157:H7
PROSPECT SHIGA TOXIN MICROPLATE ASSAY
CHROMALEX E. COLI 0157 LATEX TEST SYSTEM, PROD. NO. 800
WELLCOLEX E.COLI O157:H7
QUIX RAPID E. COLI O157 STRIP TEST
E. COLI 0157 ELISA STOOL ASSAY
E.COLI 0157 LATEX TEST
PF TEST

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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