BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    FCR DMS OPTICAL DISK IMAGE FILING UNIT OD-F614, ODF614L & MULTIMODALITY SYSTEM

    K Number: K960326 · Decision Mar 7, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    61
    Registration Numbers
    61
    Same Product Code
    54
    Applicant Total
    71
    Review Days
    43

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    Basic Information

    Device Name
    FCR DMS OPTICAL DISK IMAGE FILING UNIT OD-F614, ODF614L & MULTIMODALITY SYSTEM
    K Number
    K960326
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.2010
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Fujifilm Medical System U.S.A., Inc.
    Date Received
    January 24, 1996
    Decision Date
    March 7, 1996
    Product Code
    LMB
    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
    LMB Device, Digital Image Storage, Radiological

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