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

    HALL VEIN STRIPPER

    K Number: K872157 · Decision Jul 7, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    7
    Applicant Total
    10
    Review Days
    33

    Basic Information

    Device Name
    HALL VEIN STRIPPER
    K Number
    K872157
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4885
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    SOLCO BASLE, INC.
    Date Received
    June 4, 1987
    Decision Date
    July 7, 1987
    Product Code
    DWQ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DWQ Stripper, Vein, External

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