BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    ARTUS C. DIFFICILE QS-RGQ MDX KIT

    K Number: K133936 · Decision Apr 4, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    16
    Applicant Total
    13
    Review Days
    102

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    Basic Information

    Device Name
    ARTUS C. DIFFICILE QS-RGQ MDX KIT
    K Number
    K133936
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3130
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    QIAGEN GmbH
    Date Received
    December 23, 2013
    Decision Date
    April 4, 2014
    Product Code
    OZN
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OZN C. Difficile Toxin Gene Amplification Assay

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