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510(k) Data Aggregation

    K Number
    K980337
    Date Cleared
    1998-05-12

    (104 days)

    Product Code
    Regulation Number
    866.5100
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    DIAMEDIX IMMUNOSIMPLICITY ANA (IS-ANA) SCREEN TEST SYSTEM

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Diamedix Immunosimplicity ANA (Is-ANA) Screen is a qualitative enzyme immunoassay (EIA) intended to screen for the presence of antinuclear antibodies (ANAs) in human serum as an aid in the diagnosis of certain systemic rheumatic diseases. This assay collectively detects in one well, total ANAs against double stranded DNA (dsDNA, nDNA), Histones, SSA/Ro, SSB/La, Sm, Sm/RNP, Scl-70, Jo-1 and centromeric antigens along with sera positive for Immunofluorescent (IFA) HEp-2 ANAs. These reagents can be used either manually or in conjunction with the MAGO™ Automated EIA Processor [510(k) number K973177]. For In Vitro Diagnostic Use.

    Device Description

    The Diamedix Immunosimplicity ANA (Is-ANA) Screen is a qualitative enzyme immunoassay (EIA).

    AI/ML Overview

    I am sorry, but the provided text only contains regulatory correspondence from the FDA regarding a 510(k) premarket notification for the "Diamedix Immunosimplicity ANA (Is-ANA) Screen Test." It grants permission to market the device and describes its intended use.

    However, the document does not contain any information about acceptance criteria, device performance studies, sample sizes, ground truth establishment, expert qualifications, adjudication methods, or comparative effectiveness studies (MRMC or standalone).

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the provided input.

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