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

    VIDEO ANALYZER 4000

    K Number: K874750 · Decision Apr 25, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    54
    Registration Numbers
    54
    Same Product Code
    8
    Applicant Total
    3
    Review Days
    159

    Basic Information

    Device Name
    VIDEO ANALYZER 4000
    K Number
    K874750
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    864.3600
    Medical Specialty
    Pathology
    Decision
    Substantially Equivalent
    Applicant
    SCIENTIFIC IMAGING, INC.
    Date Received
    November 18, 1987
    Decision Date
    April 25, 1988
    Product Code
    IBJ
    Advisory Committee
    Pathology
    Review Advisory Committee
    PA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IBJ Light, Microscope

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