BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    QUIX DIGITAL RADIOGRAPHIC UPGRADE

    K Number: K052661 · Decision Jun 7, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    126
    Registration Numbers
    126
    Same Product Code
    422
    Applicant Total
    1
    Review Days
    253

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    Basic Information

    Device Name
    QUIX DIGITAL RADIOGRAPHIC UPGRADE
    K Number
    K052661
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1680
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Edge Medical Devices , Ltd.
    Date Received
    September 27, 2005
    Decision Date
    June 7, 2006
    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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