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

    VIDIVIEWER MOTORIZED MASS FILM VIEWER

    K Number: K828566 · Decision Jan 3, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    69

    Basic Information

    Device Name
    VIDIVIEWER MOTORIZED MASS FILM VIEWER
    K Number
    K828566
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    DIVERSIED P.A.
    Date Received
    October 26, 1982
    Decision Date
    January 3, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N