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510(k) Data Aggregation

    K Number
    K133005
    Date Cleared
    2014-03-13

    (169 days)

    Product Code
    Regulation Number
    864.7290
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HEMOSIL VON WILLEBRAND ACTIVITY ASSAY

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

    IL Hemosil. von Willebrand Activity is an in vitro diagnostic automated immunolurbidometric assay for the quantitative determination of von Willebrand activity in human citrated plasma on IL Coagulation Systems.

    Device Description

    Not Found

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA regarding a medical device called "HemosIL von Willebrand Activity." This document is a regulatory approval letter and indications for use, not a study report or clinical trial summary. Therefore, it does not contain the detailed information necessary to answer the questions about acceptance criteria, device performance, study design, or ground truth establishment.

    The document indicates that the device is an in vitro diagnostic automated immunoturbidometric assay for the quantitative determination of von Willebrand activity in human citrated plasma. However, it does not provide any specific performance metrics, acceptance criteria, or details of a study that proves the device meets such criteria.

    To answer your questions, I would need access to the actual 510(k) submission document or a summary of the clinical performance data, which is not present in this regulatory letter.

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