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

    COLLIMARE COLLIMATOR FAMILY

    K Number: K073124 · Decision Nov 16, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    22
    Applicant Total
    1
    Review Days
    10

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    Basic Information

    Device Name
    COLLIMARE COLLIMATOR FAMILY
    K Number
    K073124
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    892.1610
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Collimare, LLC
    Date Received
    November 6, 2007
    Decision Date
    November 16, 2007
    Product Code
    IZW
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    IZW Collimator, Automatic, Radiographic

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