BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

    CORONIS 5MP MAMMO SL, MODEL MDMG 6121

    K Number: K081109 · Decision May 2, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    5
    Review Days
    14

    Basic Information

    Device Name
    CORONIS 5MP MAMMO SL, MODEL MDMG 6121
    K Number
    K081109
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    BARCOVIEW, MEDICAL IMAGING SYSTEMS
    Date Received
    April 18, 2008
    Decision Date
    May 2, 2008
    Product Code
    LLZ
    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
    LLZ System, Image Processing, Radiological

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

    CustomSurg OrthoPlanner

    FDA 510(k)
    FDA Class 2 ·Radiology

    uOmniscan

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mosaic (V1.0.1)

    FDA 510(k)
    FDA Class 2 ·Radiology

    UroNav 4

    FDA 510(k)
    FDA Class 2 ·Radiology

    TechLive

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMARTDent

    FDA 510(k)
    FDA Class 2 ·Radiology
    View all

    Other Clearances by BARCOVIEW, MEDICAL IMAGING SYSTEMS

    K Number Device Name
    K073007 CORONIS FUSION 6MP DL, MODEL: MDCC 6130 DL
    K072875 NIO 5MP DISPLAY, MODEL E5620
    K073205 NIO 5MP, MODEL MDNG-5121
    K070726 NIO COLOR 3MP AND MDNC 3120