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

    TRI-FLOW THREE WAY STOPCOCK

    K Number: K961982 · Decision Feb 21, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    93
    Registration Numbers
    93
    Same Product Code
    88
    Applicant Total
    2
    Review Days
    277

    Basic Information

    Device Name
    TRI-FLOW THREE WAY STOPCOCK
    K Number
    K961982
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    NORTH, INC.
    Date Received
    May 20, 1996
    Decision Date
    February 21, 1997
    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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