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    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

    QANGIO CT

    K Number: K062386 · Decision Oct 5, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    163
    Registration Numbers
    163
    Same Product Code
    818
    Applicant Total
    17
    Review Days
    51

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    Basic Information

    Device Name
    QANGIO CT
    K Number
    K062386
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1750
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medis Medical Imaging Systems BV
    Date Received
    August 15, 2006
    Decision Date
    October 5, 2006
    Product Code
    JAK
    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
    JAK System, X-Ray, Tomography, Computed

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