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

    ELECTROLYTES (NA+, K+, CL-), PRODUCT NO'S 114-01, 114-02, 114-03

    K Number: K991870 · Decision Jul 30, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    37
    Applicant Total
    18
    Review Days
    59

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    Basic Information

    Device Name
    ELECTROLYTES (NA+, K+, CL-), PRODUCT NO'S 114-01, 114-02, 114-03
    K Number
    K991870
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1170
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    A.P. Total Care, Inc.
    Date Received
    June 1, 1999
    Decision Date
    July 30, 1999
    Product Code
    CGZ
    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
    CGZ Electrode, Ion-Specific, Chloride

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    Other Clearances by A.P. Total Care, Inc.

    K Number Device Name
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    K991761 MAGNESIUM PRODUCT NO'S, 112-01, 112-02
    K991664 LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01
    K991665 HDL CHOLESTEROL, PRODUCT NO'S 124-01, CH102-01
    K991867 INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02
    K991866 BILIRUBIN, TOTAL AND DIRECT, PRODUCT NO, 122-01, 122-02, 122-03, 122-04
    K991663 AST/SGOT
    K991666 TIBC, PRODUCT NO'S 123-0, 123-02, FE109-01, FE109-02
    K991247 URIC ACID, MODEL UA112-01
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