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

    KEMTROL SERUM CONTROL ABNORMAL

    K Number: K802109 · Decision Oct 10, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    135
    Registration Numbers
    135
    Same Product Code
    672
    Applicant Total
    280
    Review Days
    37

    Basic Information

    Device Name
    KEMTROL SERUM CONTROL ABNORMAL
    K Number
    K802109
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1660
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    HELENA LABORATORIES
    Date Received
    September 3, 1980
    Decision Date
    October 10, 1980
    Product Code
    JJY
    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
    JJY Multi-Analyte Controls, All Kinds (Assayed)

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