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

    IL PHOENIX, MODEL 900, CHEMISTRY/ELECTROLYTE ANALY

    K Number: K884771 · Decision Feb 10, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    33
    Registration Numbers
    33
    Same Product Code
    28
    Applicant Total
    321
    Review Days
    88

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    Basic Information

    Device Name
    IL PHOENIX, MODEL 900, CHEMISTRY/ELECTROLYTE ANALY
    K Number
    K884771
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1145
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Instrumentation Laboratory CO
    Date Received
    November 14, 1988
    Decision Date
    February 10, 1989
    Product Code
    JFP
    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
    JFP Electrode, Ion Specific, Calcium

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