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

    C-SECTION TRAY

    K Number: K912075 · Decision Apr 7, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    57
    Applicant Total
    30
    Review Days
    333

    Basic Information

    Device Name
    C-SECTION TRAY
    K Number
    K912075
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    MEDICAL DEVICE INSPECTION CO., INC.
    Date Received
    May 10, 1991
    Decision Date
    April 7, 1992
    Product Code
    KNA
    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
    KNA Instrument, Manual, Specialized Obstetric-Gynecologic

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