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

    FLAME PHOTOMETER, MODEL 455

    K Number: K780650 · Decision May 26, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    21
    Applicant Total
    111
    Review Days
    37

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    Basic Information

    Device Name
    FLAME PHOTOMETER, MODEL 455
    K Number
    K780650
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2540
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Corning Medical & Scientific
    Date Received
    April 19, 1978
    Decision Date
    May 26, 1978
    Product Code
    JJO
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JJO Flame Emission Photometer For Clinical Use

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