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

    VISIONLINK INTERFILE CONVERSION SOFTWARE

    K Number: K933372 · Decision Nov 1, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    85
    Registration Numbers
    85
    Same Product Code
    470
    Applicant Total
    7
    Review Days
    115

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    Basic Information

    Device Name
    VISIONLINK INTERFILE CONVERSION SOFTWARE
    K Number
    K933372
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1200
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Evergreen Technologies, Inc.
    Date Received
    July 9, 1993
    Decision Date
    November 1, 1993
    Product Code
    KPS
    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
    KPS System, Tomography, Computed, Emission

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    Other Clearances by Evergreen Technologies, Inc.

    K Number Device Name
    K942861 MEDVISION ENVIROMENT/MEDVISION 2.0
    K942860 VISIONLINK DICOM MODULE
    K935103 VISIONLINK ACR-NEMA CONVERSION UTILITIES
    K933209 VISIONTOOL
    K924178 MEDVISION(TM) IMAGING SOFTWARE
    K921484 MEDVISION