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510(k) Data Aggregation

    K Number
    K140761
    Device Name
    KAHN UTERINE CANNULA, JARCHO UTERINE CANNULA, NEAL FALLOPIAN CANNULA
    Manufacturer
    CAREFUSION 2200 INC.
    Date Cleared
    2014-04-21

    (26 days)

    Product Code
    HES
    Regulation Number
    884.1300
    Why did this record match?
    Product Code :

    HES

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Kahn Uterine Trigger Cannula, Jarcho Self-Retaining Uterine Cannula, and Neal Fallopian Cannula are indicated to test the patency (lack of obstruction) of the fallopian tubes by pressurizing the uterus and filling them with carbon dioxide gas.
    Device Description
    The V. Mueller® Uterine Cannula devices are constructed with a stopcock, finger ring control, an elongate shaft and a distal end with a rubber acorn.
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    K Number
    K000340
    Device Name
    HYSTALOG HSG CATHETER
    Manufacturer
    ROCKET MEDICAL PLC
    Date Cleared
    2000-04-19

    (76 days)

    Product Code
    HES
    Regulation Number
    884.1300
    Why did this record match?
    Product Code :

    HES

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question

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