BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    M. DIOR BRAND

    K Number: K083817 · Decision Sep 16, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    400
    Applicant Total
    2
    Review Days
    268

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    Basic Information

    Device Name
    M. DIOR BRAND
    K Number
    K083817
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    884.5300
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Suzhou Colour-Way Enterprise Development Co., Ltd.
    Date Received
    December 22, 2008
    Decision Date
    September 16, 2009
    Product Code
    HIS
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HIS Condom

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    Other Clearances by Suzhou Colour-Way Enterprise Development Co., Ltd.

    K Number Device Name
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