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510(k) Data Aggregation

    K Number
    K032535
    Date Cleared
    2003-09-10

    (23 days)

    Product Code
    Regulation Number
    866.5775
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    MODIFICATION TO:ROCHE DIAGNOSTICS TINA-QUANT RHEUMATOID FACTORS II TEST SYSTEM

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

    Immunoturbidimetric assay for the in vitro quantitative determination of rheumatoid factors in human serum and plasma on automated clinical chemistry analyzers. Measurements may be used as an aid in the diagnosis of rheumatoid arthritis.

    Device Description

    The Tina-quant® Rheumatoid Factors II Test System is a particle enhanced immunoturbidimetric assay. Latex-bound heat inactivated IgG (antigen) reacts with the RF-antibodies in the sample to form antigen/antibody complexes which, following agglutination, are measured turbidimetrically.

    AI/ML Overview

    The provided text is a 510(k) summary for the Tina-quant® RF II Test System, a medical device for in vitro diagnostic use. It describes the device, its intended use, and claims substantial equivalence to a previously marketed device. However, it does not contain information about acceptance criteria, a study proving the device meets those criteria, or any of the detailed study parameters requested in the prompt.

    Therefore, I cannot provide the requested information from the given text. The document is primarily a regulatory submission, not a detailed study report.

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