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: LLM FDA class 1

Test, Antigen, Nuclear, Epstein-Barr Virus

Microbiology

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Test, Antigen, Nuclear, Epstein-Barr Virus is a diagnostic test used to detect the Epstein-Barr Virus Nuclear Antigen (EBNA), which appears in infected cells following EBV infection and whose presence indicates past rather than acute EBV infection, aiding in the serological staging of EBV-related disease. This device is classified as FDA Class 1, the lowest risk category, requiring only general controls. The product code is LLM, regulated under 21 CFR 866.3235, within the Microbiology medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

27 matches
K Number
Device Name
ADVIA Centaur EBV-EBNA IgG
DIASORIN LIAISON EBNA IGG, LIAISON VCA IGG, LIAISON VCA IGM ASSAYS
THE APTUS (AUTOMATED) APPLICATION OF THE EBNA IGG ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR TH
IMMUNOWELL EBNA IGG TEST
EBNA-1 IGM ELISA TEST SYSTEM
EBNA IGG EIA TEST SYSTEM
EBNA ENZYME IMMUNOASSAY KIT
EBNA IGG ELISA TEST
EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN RECOMBINANT IMMUNOFLUORESCENT ASSAY
INCSTAR EPSTEIN-BARR NUCLEAR ANTIGEN (EBNA_ IGG ELISA KIT
EBNA IGG ELISA TEST SYSTEM
MERIDIAN EBNA TEST KIT
ORTHO*EPSTEIN-BARR VIRUS EBNA-IFF ANTIBODY ELISA
EBNA STAT TEST KIT
EPSTEIN-BARR VIRUS EBNA-IGG ANTIBODY ELISA TEST
EBNA ANTIBODY TEST SYSTEM (IMMUNOFLUORESCENT ANTI)
EBNA ANTIBODY TEST SYSTEM (IMMUNOENZYME ANTIBODY)
EPSTEIN-BARR VIRUS-NUCLEAR ANTIGEN
EBNA-CHECK(TM) TEST KIT
EPSTEIN-BARR VIRUS (EBNA-1) IGM CATA. #5550
EPSTEIN-BARR VIRUS (EBNA-1) IGG CATA. #4550
EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN ANTIBODY TEST
DU PONT EBNA-IGG ANTIBODY ELISA KIT
EBNA ANTIBODY
EBV-NA TEST
EBNA ACIF ASSAY KIT
EBNA ACIF KIT

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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