BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

    Double Lumen Ovum Aspiration Needles

    K Number: K171611 · Decision Dec 15, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    27
    Registration Numbers
    27
    Same Product Code
    32
    Applicant Total
    14
    Review Days
    197

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    Basic Information

    Device Name
    Double Lumen Ovum Aspiration Needles
    K Number
    K171611
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    884.6100
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    William A. Cook Australia Pty. , Ltd.
    Date Received
    June 1, 2017
    Decision Date
    December 15, 2017
    Product Code
    MQE
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MQE Needle, Assisted Reproduction

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