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

    INSUFFLATION NEEDLE- 120MM, MODEL 900-200

    K Number: K993625 · Decision Jun 20, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    176
    Applicant Total
    6
    Review Days
    238

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    Basic Information

    Device Name
    INSUFFLATION NEEDLE- 120MM, MODEL 900-200
    K Number
    K993625
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1730
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Genicon, LC
    Date Received
    October 26, 1999
    Decision Date
    June 20, 2000
    Product Code
    HIF
    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
    HIF Insufflator, Laparoscopic

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