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

    DIRECT DIGITIZER, REGIUS MODEL 210

    K Number: K092717 · Decision Oct 30, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    126
    Registration Numbers
    126
    Same Product Code
    422
    Applicant Total
    27
    Review Days
    57

    Basic Information

    Device Name
    DIRECT DIGITIZER, REGIUS MODEL 210
    K Number
    K092717
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1680
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Konica Minolta Medical & Graphic, Inc.
    Date Received
    September 3, 2009
    Decision Date
    October 30, 2009
    Product Code
    MQB
    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
    MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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