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

    SONY CINE VIDEO SYSTEM SME-3500

    K Number: K904447 · Decision Oct 17, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    123
    Registration Numbers
    123
    Same Product Code
    198
    Applicant Total
    8
    Review Days
    19

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    Basic Information

    Device Name
    SONY CINE VIDEO SYSTEM SME-3500
    K Number
    K904447
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1600
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Sony Medical Electronics Co.
    Date Received
    September 28, 1990
    Decision Date
    October 17, 1990
    Product Code
    IZI
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IZI System, X-Ray, Angiographic

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