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510(k) Data Aggregation

    K Number
    K040560
    Manufacturer
    Date Cleared
    2004-07-27

    (146 days)

    Product Code
    Regulation Number
    866.1640
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ETEST FOR ANTIFUNGAL SUSCEPTTIBILITY TESTING

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

    Etest® is an agar-based gradient technique for quantitative antifungal susceptibility testing of Candida species. It uses a predefined concentration gradient of the specific antifungal agent to determine the Minimum Inhibitory Concentration (MIC) in ug/mL inhibiting the growth of the test organism under defined conditions. This 510k submission is for an application for in wire diagnostic use of Etest for MIC determination of fluconazole, itraconazole and flucytosine with Candida species.

    Device Description

    Not Found

    AI/ML Overview

    The provided document is an FDA 510(k) clearance letter for an antimicrobial susceptibility test. It does not contain the detailed study information, acceptance criteria, or performance data typically found in a clinical study report or a more comprehensive submission document.

    Therefore, I cannot extract the information required in the prompt (acceptance criteria, reported device performance, sample size, data provenance, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, standalone performance, training set details) from this letter.

    The letter primarily confirms that the device is substantially equivalent to a legally marketed predicate device for the stated indications for use. It doesn't present the underlying data or the specific criteria against which that data was evaluated.

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