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

    MODEL 410 DENTAL X-RAY FILM PROCESSORS

    K Number: K874118 · Decision Nov 6, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    8
    Applicant Total
    1
    Review Days
    28

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    Basic Information

    Device Name
    MODEL 410 DENTAL X-RAY FILM PROCESSORS
    K Number
    K874118
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1900
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Dent-X Co.
    Date Received
    October 9, 1987
    Decision Date
    November 6, 1987
    Product Code
    EGY
    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
    EGY Processor, Radiographic-Film, Automatic, Dental

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