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

    MIRAGE CEDARS OPTION

    K Number: K070683 · Decision Apr 12, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    4
    Review Days
    31

    Basic Information

    Device Name
    MIRAGE CEDARS OPTION
    K Number
    K070683
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    SEGAMI CORPORATION
    Date Received
    March 12, 2007
    Decision Date
    April 12, 2007
    Product Code
    LLZ
    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
    LLZ System, Image Processing, Radiological

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    Other Clearances by SEGAMI CORPORATION

    K Number Device Name
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