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

    KNAI SODIUM POTASSIUM ANALYZER

    K Number: K830805 · Decision Apr 8, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    208
    Applicant Total
    50
    Review Days
    25

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    Basic Information

    Device Name
    KNAI SODIUM POTASSIUM ANALYZER
    K Number
    K830805
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2300
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Radiometer America, Inc.
    Date Received
    March 14, 1983
    Decision Date
    April 8, 1983
    Product Code
    JSG
    Advisory Committee
    Microbiology
    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
    JSG Culture Media, Non-Selective And Non-Differential

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