BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

    POWDERED LATEX SURGEON'S GLOVE

    K Number: K121925 · Decision Aug 28, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    138
    Registration Numbers
    138
    Same Product Code
    558
    Applicant Total
    2
    Review Days
    422

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    Basic Information

    Device Name
    POWDERED LATEX SURGEON'S GLOVE
    K Number
    K121925
    Device Class
    FDA class 1
    Clearance Type
    Abbreviated
    Regulation Number
    878.4460
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Suzhou Colour-Way Enterprise Development Co., Ltd.
    Date Received
    July 2, 2012
    Decision Date
    August 28, 2013
    Product Code
    KGO
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KGO Surgeon'S Gloves

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

    K Number Device Name
    K083817 M. DIOR BRAND