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

    APPOSE SKIN STAPLER & REMOVER

    K Number: K823552 · Decision Jun 15, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    136
    Registration Numbers
    136
    Same Product Code
    282
    Applicant Total
    7
    Review Days
    197

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    Basic Information

    Device Name
    APPOSE SKIN STAPLER & REMOVER
    K Number
    K823552
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4750
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    American Cyanamid Co.
    Date Received
    November 30, 1982
    Decision Date
    June 15, 1983
    Product Code
    GDW
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GDW Staple, Implantable

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