BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    TOMTEC-ARENA TTA2

    K Number: K150122 · Decision Feb 13, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    18
    Review Days
    24

    Basic Information

    Device Name
    TOMTEC-ARENA TTA2
    K Number
    K150122
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    TOMTEC IMAGING SYSTEMS, GMBH
    Date Received
    January 20, 2015
    Decision Date
    February 13, 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 TOMTEC IMAGING SYSTEMS, GMBH

    K Number Device Name
    K132544 TOMTEC-ARENA 1.0, TOMTEC-ARENA 3D ECHO, CARDIO-ARENA
    K120135 2D CARDIAC PERFORMANCE ANALYSIS MR 1.0
    K110746 4D LV-ANALYSIS 3.0
    K110667 IMAGE-ARENA AND IMAGE-ARENA APPLICATIONS
    K110595 4D SONO-SCAN 1.0
    K103782 4D MV-ASSESSMENT 2.0
    K090461 IMAGE-ARENA 4.0 AND IA APPLICATIONS 2D CARDIAC PERFORMANCE ANALYSIS 1.0
    K083348 IMAGE-ARENA APPLICATIONS
    K082510 IMAGE-ARENA APPLICATIONS, MODEL IMAGE-ARENA VA PLATFORM 1.0, 4D LV-ANALYSIS 2.5, 4D LV-ANALYSIS MR 1.0
    K071232 IMAGE-ARENA APPLICATIONS AND RESEARCH-ARENA APPLICATIONS
    Search all 18 clearances from TOMTEC IMAGING SYSTEMS, GMBH →