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510(k) Data Aggregation

    K Number
    K051307
    Date Cleared
    2005-06-13

    (25 days)

    Product Code
    Regulation Number
    862.3170
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Benzodiazepine (BENZ) Reagent, in conjunction with SYNCHRON® Systems Drugs of Abuse Testing (DAT) Urine Calibrators, is intended for the qualitative determination of benzodiazepines in human urine at a cutoff value of 200 ng/mL (oxazepam), on SYNCHRON Systems.

    The Benzodiazepine assay provides a rapid screening procedure for determining the presence of benzodiazepines in urine. This test provides only a preliminary analytical result; a positive result by this assay should be confirmed by another generally accepted non-immunological method, such as thin layer chromatography (TLC), gas chromatography (GC), or gas chromatography/mass spectrometry (GC/MS). GC/MS is the preferred confirmatory method.

    Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

    Device Description

    The SYNCHRON Systems Benzodiazepine (BENZ) reagent is designed for optimal performance on the SYNCHRON CX (CX4/4CE/4A/4PRO, CX5/5CE/5Δ/5PRO, CX7/7RTS/7Δ/7PRO, CX9ALX/9PRO, LX20/PRO, and UniCel DxC 600/800 Systems. The reagent kit contains one 250-test cartridge that is packaged separately from the associated calibrators.

    AI/ML Overview

    The provided text is a 510(k) summary for the SYNCHRON Systems Benzodiazepine Reagent. It mentions a modification to the predicate device and states that "Performance data from validation testing supports equivalency." However, it does not include the detailed performance data or a study report with acceptance criteria.

    Therefore, I cannot populate the requested table and answer the study-related questions based on the provided document alone. The summary explicitly states "Summary of Performance Data Performance data from validation testing supports equivalency," but does not present that data or the acceptance criteria.

    To fulfill your request, I would need access to the actual validation testing report that was submitted with the 510(k).

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