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: LJN FDA class 1

Antibody Igm, If, Epstein-Barr Virus

Microbiology

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Antibody IgM, If, Epstein-Barr Virus is an immunofluorescence (IF) assay reagent used in clinical microbiology laboratories to detect IgM-class antibodies against Epstein-Barr Virus (EBV), aiding in the diagnosis of primary EBV infection such as infectious mononucleosis. This is an FDA Class 1 device, the lowest risk category, subject to general controls only. The product code is LJN, regulated under 21 CFR 866.3235, within the Microbiology medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

23 matches
K Number
Device Name
BIOPLEX 2200 EBV IGM KIT
PLEXUS EBV IGM MULTI-ANALYTE DIAGNOSTICS, MODEL: MP0600M
ATHENA MULTI-LYTE EBV VCA IGM TEST SYSTEM
MODIFICATION TO SERAQUEST VCA IGM
SERAQUEST EB VAC IGM
COPALIS EBV-M ANTIBODY ASSAY
IMMUNOWELL VCA IGM TEST
EPSTEIN-BARR VIRUS VCA (IGM) RECOMB IMMUN ANTIBODY
ORTHO*EPSTEIN-BARR VIRUS VCA-IGM ANTIBODY ELISA
BARTELS EPSTEIN-BARR VIRUS IGM EIA
EBV-VCA IGM ELISA
AMIZYME EPSTEIN-BARR VIRUS (EBV) IGM ANTIBODY TEST
EBV IGM ELISA TEST
(EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM
EBV VCA ANTIBODY (IGM)
BION EBV-M (VCA) TEST SYSTEM
RESUBMITTED EBV/IGM-CHECK TEST KIT
EBV-VCA IGM ANTIBODY TEST SYSTEM (ENZYME)
EBV-VCA IGM ANTIBODY TEST SYSTEM (FLUORESCENT)
DU PONT VCA-IGM ANTIBODY ELISA KIT
ORTHO MONOLERT* RAPID ELISA TEST FOR INFECT. MONO.
EBV VCA IGM ANTIBODY ASSAY KIT
EBV-VCA-IGM IFA TEST SYSTEM

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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