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

    4-WAY STOPCOCK W/10 CM EXTEN. TUBING

    K Number: K760667 · Decision Dec 2, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    88
    Applicant Total
    10
    Review Days
    76

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    Basic Information

    Device Name
    4-WAY STOPCOCK W/10 CM EXTEN. TUBING
    K Number
    K760667
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    American Viggo
    Date Received
    September 17, 1976
    Decision Date
    December 2, 1976
    Product Code
    FMG
    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
    FMG Stopcock, I.V. Set

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