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    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

    ARGOS

    K Number: K061479 · Decision Apr 5, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    250
    Registration Numbers
    250
    Same Product Code
    422
    Applicant Total
    2
    Review Days
    310

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    Basic Information

    Device Name
    ARGOS
    K Number
    K061479
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.4560
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    3D Line Medical Systems S.R.L.
    Date Received
    May 30, 2006
    Decision Date
    April 5, 2007
    Product Code
    HAW
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    HAW Neurological Stereotaxic Instrument

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    Other Clearances by 3D Line Medical Systems S.R.L.

    K Number Device Name
    K080601 ERGO++ VERSION 1.7