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

    VIGGO ARTERIAL CANNULA

    K Number: K850349 · Decision Apr 9, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    212
    Registration Numbers
    213
    Same Product Code
    496
    Applicant Total
    7
    Review Days
    71

    Basic Information

    Device Name
    VIGGO ARTERIAL CANNULA
    K Number
    K850349
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    VIGGO PRODUCTS
    Date Received
    January 28, 1985
    Decision Date
    April 9, 1985
    Product Code
    FOZ
    Advisory Committee
    General Hospital
    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
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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    Other Clearances by VIGGO PRODUCTS

    K Number Device Name
    K850769 VIGGO ACCESSORIES FOR I.V. THERAPY
    K850276 VIGGO NEOFLON INFUSION CANNULA
    K850277 VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.
    K850460 VIGGO SECALON T CATHETER
    K850280 VIGGO CONNECTA 3-WAY INFUSION STOPCOCK
    K850278 VASCULON I.V. CANNULAE