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: GNP FDA class 1

Antiserum, Cf, Epstein-Barr Virus

Microbiology

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The Epstein-Barr Virus CF (Complement Fixation) Antiserum is a reference reagent used in complement fixation tests for the serological detection of Epstein-Barr virus (EBV), the causative agent of infectious mononucleosis and a virus associated with several malignancies. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is GNP, regulated under 21 CFR 866.3235 in the Microbiology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

20 matches
K Number
Device Name
EBV V VCA IGM ELISA KIT MODEL# EBM-200
EBV-VCA IGG ELISA TEST, MODEL EBG-100
EBV-EBNA IGG ELISA KIT, MODEL EBG-100
IS EBV-EBNA-1 IGG ELISA TEST SYSTEM
IS EBV-EA-D IGG ELISA TEST SYSTEM
EIA FOR IGG ANTIBODY TO EBV VCA IN HUMAN SERUM
SEROLOGICAL TEST KIT FOR IGG ANTI. EPSTEIN-BARR VI
EBV-VCA ANTIBODY (IGG)
EBV-VCA IGG ANTIBODY TEST SYSTEM (ENZYME)
EBV-VCA IGG ANTIBODY TEST SYSTEM (FLUORESCENT)
EBV-CHECK(TM) TEST KIT (IGG)
THE GOLDEN QUAD TEST (EBV)
INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCA
EBV/VCA-CHECK(TM) ANTIGEN SLIDES
EBV(EPSTEIN-BARR VIRUS) TEST KIT
INDIRECT ENZYME LINKED IMMUNOSORBENT ASSAY IGG ANT
ANTI-EPSTEIN-BARR VIRUS KIT
AMIZYME-EBV TEST KIT
ENI ANTIBODY TO EPSTEIN-BARR VIRUS
EBV 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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