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

    VOSS VEIN CLAMP

    K Number: K885161 · Decision Dec 22, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    186
    Registration Numbers
    186
    Same Product Code
    203
    Applicant Total
    5
    Review Days
    374

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    Basic Information

    Device Name
    VOSS VEIN CLAMP
    K Number
    K885161
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Voss Medical Products
    Date Received
    December 13, 1988
    Decision Date
    December 22, 1989
    Product Code
    DXC
    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
    DXC Clamp, Vascular

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    Other Clearances by Voss Medical Products

    K Number Device Name
    K932187 PRONE POSITIONER
    K932186 BYPASS LEG POSITIONER
    K896338 VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA
    K895369 VOSS GRAFT MARKER