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

    UNISCAN, PULMOSCAN, PULMOSCAN RADIOGRAPHIC SYSTEMS

    K Number: K033577 · Decision Mar 18, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    355
    Applicant Total
    1
    Review Days
    491

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    Basic Information

    Device Name
    UNISCAN, PULMOSCAN, PULMOSCAN RADIOGRAPHIC SYSTEMS
    K Number
    K033577
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    892.1680
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medlink Imaging
    Date Received
    November 13, 2003
    Decision Date
    March 18, 2005
    Product Code
    KPR
    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
    KPR System, X-Ray, Stationary

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