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

    PILLING BRUSH VALVULOTOME

    K Number: K904507 · Decision Mar 1, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    7
    Applicant Total
    39
    Review Days
    150

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    Basic Information

    Device Name
    PILLING BRUSH VALVULOTOME
    K Number
    K904507
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4885
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Pilling Co.
    Date Received
    October 2, 1990
    Decision Date
    March 1, 1991
    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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