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

    4-WAY STOPCOCK W/LUER-LOCK FITTING

    K Number: K760666 · 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/LUER-LOCK FITTING
    K Number
    K760666
    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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    Other Clearances by American Viggo

    K Number Device Name
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    K770154 3-WAY STOPCOCK WITH LUER-LOCK FITTING
    K770096 EPIDURAL BLOCK PROCEDURE PACK
    K760679 4-WAY STOPCOCK W/7CM TUBING,
    K760678 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK
    K760667 4-WAY STOPCOCK W/10 CM EXTEN. TUBING