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: MVM FDA class 2

Autoantibodies, Endomysial(Tissue Transglutaminase)

Immunology

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An Endomysial/Tissue Transglutaminase Autoantibody Test is an immunological in vitro diagnostic device that detects autoantibodies against endomysial antigens or tissue transglutaminase in serum, used as a highly specific serological marker for the diagnosis of celiac disease and dermatitis herpetiformis. It is FDA Class 2, requiring 510(k) clearance, with product code MVM under 21 CFR 866.5660 in the Immunology specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

40 matches
K Number
Device Name
Aptiva Celiac Disease IgG Reagent
Aptiva Celiac Disease IgA Reagent
EliA Celikey IgG Immunoassay; EliA GliadinDP IgA Immunoassay; EliA GliadinDP IgG Immunoassay
EUROIMMUN Anti-tissue Transglutaminase ELISA (IgA), EUROIMMUN Anti-tissue Transglutaminase ELISA (IgG)
IG_PLEX CELIAC DGP PANEL
IMMULISA ENHANCED CELIAC FUSION (TTG/DGP) IGA/IGG ANTIBODY ELISA
BIOPLEX 2200 CELIAC IGA AND IGG KITS ON THE BIOPLEX 2200 SYSTEM, BIOPLEX 2200 CELIAC IGA AND IGG CALIBRATOR SETS, AND BI
IGX PLEX CELIAC QUALITATIVE ASSAY
QUANTA FLASH H-TTG IGG
EU-TTG IGA AND EU-TTG IGG
QUANTA FLASH H-TTG IGA
IMMULISA CELIAC TTG IGA AND IGG ANTIBODY ELISA
QUANTA LITE H-TTG SCREEN
QUANTA PLEX CELIAC IGG PROFILE
QUANTA LITE F-ACTIN IGA ELISA
THERATEST EL-TTG IGA/IGG AND THERATEST EL-GLIA IGA/IGG TEST SYSTEMS
QUANTA PLEX CELIAC IGA PROFILE
ELIA CELIKEY IGA WELL, MODEL 14-5517-01; ELIA CELIAC CONTROL, MODEL 83-1011-01
ELIA CELIKEY IGG WELL, MODEL 14-5518-01, ELIA CELIAC CONTROL, MODEL 83-1011-01
EUROIMMUN ENDOMYSIUM IFA: ESOPHAGUS (MONKEY) KIT
IMMUGLO ANTI-ENDOMYSIAL ANTIBODY IFA
AESKULISA TTG A AND AESKULISA TTG G
AUTOSTAT II ANTI-TISSUE TRANSGLUTAMINASE IGG ELISA
CELIKEY IGG ITG IGG ANTIBODIES, MODEL 17996
CELIKEY TTG (HUMAN, RECOMBINANT) IGA ANTIBODIES MODEL #18148/18196
BINDAZYME HUMAN ANTI TISSUE TRANSGLUTAMINASE IGA AND IGG EIA DIAGNOSTIC TEST KITS
IMMULISA ANTI-HUMAN TISSUE TRANSGLUTAMINASE (HU-TTG) ANTIBODY TOTAL IGA/IGG ELISA
AUTOSTAT II ANTI-TISUE TRANSGLUTAMINASE IGA ELISA
IMMULISA ANTI-HUMAN TISSUE TRANSGLUTAMINASE (HU-TTG) ANTIBODY IGA ELISA
QUANTA LITE H-TTG (HUMAN TISSUE TRANSGLUTAMINASE) IGA ELISA
QUANTA LITE H-TTG (HUMAN TISSUE TRANSGLUTAMINASE) IGG ELISA
EUROSPITAL EU-TTG IGA UMANA
IFA KIT FOR THE DETECTION OF ENDOMYSIAL IGA ANIBODIES USING PRIMATE UMBILICAL CORD (PUC)-EMA/PUC LGA.
EU-TTG IGA ELISA
BINDAZYME ANTI-TISSUE TRANSGLUTAMINASE IGA EIA
MEDICA INDIRECT IMMUNOFLUORESCENCE (IIF) ANTI- ENDOMYSIAL ANTIBODY (AEMA) TEST KIT, MODEL 6001-ESD
ANTI-TISSUE TRANSGLUTAMINASE (TTG)ANTIBODY TEST
QUANTA LITE CELIAC SCREEN (TISSUE TRANSGLUTAMINASE/GLIADIN) ELISA
MONKEY OESOPHAGUS IFA DIAGNOSTIC TEST KITS
QUANTA LITE TTG (TISSUE TRANSGLUTAMINASE) ELISA

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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