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

    VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.

    K Number: K850277 · Decision Apr 12, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    7
    Review Days
    79

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    Basic Information

    Device Name
    VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.
    K Number
    K850277
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Viggo Products
    Date Received
    January 23, 1985
    Decision Date
    April 12, 1985
    Product Code
    FPA
    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
    FPA Set, Administration, Intravascular

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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
    K850460 VIGGO SECALON T CATHETER
    K850280 VIGGO CONNECTA 3-WAY INFUSION STOPCOCK
    K850349 VIGGO ARTERIAL CANNULA
    K850278 VASCULON I.V. CANNULAE