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

    VARIVIEWER (X-RAY FILM VIEWER)

    K Number: K875233 · Decision Jan 19, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    17
    Applicant Total
    1
    Review Days
    28

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    VARIVIEWER (X-RAY FILM VIEWER)
    K Number
    K875233
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1890
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Diversified Diagnostic Products, Inc.
    Date Received
    December 22, 1987
    Decision Date
    January 19, 1988
    Product Code
    IXC
    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
    IXC Illuminator, Radiographic-Film

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (IXC), ordered by most recent decision date.

    SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUS

    FDA 510(k)
    FDA Class 1 ·Radiology

    SMART MOTORIZED VIEWER

    FDA 510(k)
    FDA Class 1 ·Radiology

    ARRIPRO 35 ST/TV

    FDA 510(k)
    FDA Class 1 ·Radiology

    DIFFUSER PANEL

    FDA 510(k)
    FDA Class 1 ·Radiology

    LILY DARK VIEWER

    FDA 510(k)
    FDA Class 1 ·Radiology

    VOXBOX

    FDA 510(k)
    FDA Class 1 ·Radiology
    View all