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

    URIC ACID REAGENT SET

    K Number: K760989 · Decision Dec 9, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    30
    Applicant Total
    13
    Review Days
    34

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    Basic Information

    Device Name
    URIC ACID REAGENT SET
    K Number
    K760989
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1775
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Worthington Biochemical Corp.
    Date Received
    November 5, 1976
    Decision Date
    December 9, 1976
    Product Code
    CDO
    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
    CDO Acid, Uric, Uricase (U.V.)

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    Other Clearances by Worthington Biochemical Corp.

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    K772025 URIC ACID STD. FOR QUANT. URIC ACID
    K771001 STATZYME GLUCOSE
    K771143 INORGANIC PHOSPHORUS STANDARDS
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