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

    TRACTUS TISSUEMAPPER REVIEWER APPLICATION

    K Number: K123901 · Decision Jan 29, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    2
    Review Days
    42

    Basic Information

    Device Name
    TRACTUS TISSUEMAPPER REVIEWER APPLICATION
    K Number
    K123901
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    TRACTUS CORPORATION
    Date Received
    December 18, 2012
    Decision Date
    January 29, 2013
    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

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    Other Clearances by TRACTUS CORPORATION

    K Number Device Name
    K131489 TRACTUS TISSUEMAPPER IMAGE RECORDING SYSTEM APPLICATION