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

    RAPID AUTOMATIC PNEUMOPERITONEUM-I

    K Number: K900808 · Decision Sep 19, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    176
    Applicant Total
    8
    Review Days
    210

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    Basic Information

    Device Name
    RAPID AUTOMATIC PNEUMOPERITONEUM-I
    K Number
    K900808
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1730
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Trek Medical Products, Inc.
    Date Received
    February 21, 1990
    Decision Date
    September 19, 1990
    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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