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

    CALCIUM AND PH ELECTROLYTE ANALYZER

    K Number: K895397 · Decision Dec 12, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    33
    Registration Numbers
    33
    Same Product Code
    28
    Applicant Total
    7
    Review Days
    102

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    Basic Information

    Device Name
    CALCIUM AND PH ELECTROLYTE ANALYZER
    K Number
    K895397
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1145
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Ionetics, Inc.
    Date Received
    September 1, 1989
    Decision Date
    December 12, 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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