BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    McKesson Radiology Mammography Plus

    K Number: K142850 · Decision Jan 6, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    3
    Review Days
    98

    Basic Information

    Device Name
    McKesson Radiology Mammography Plus
    K Number
    K142850
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    MCKESSON MEDICAL IMAGING COMPANY
    Date Received
    September 30, 2014
    Decision Date
    January 6, 2015
    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 MCKESSON MEDICAL IMAGING COMPANY

    K Number Device Name
    K140909 MCKESSON RADIOLOGY
    K043146 HORIZON MEDICAL IMAGING