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

    U.S. DIAGNOSTICS ENZYMATIC TRIGLYCERIDE TEST

    K Number: K864231 · Decision Dec 4, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    150
    Applicant Total
    22
    Review Days
    37

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    Basic Information

    Device Name
    U.S. DIAGNOSTICS ENZYMATIC TRIGLYCERIDE TEST
    K Number
    K864231
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1705
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    U. S. Diagnostics, Inc.
    Date Received
    October 28, 1986
    Decision Date
    December 4, 1986
    Product Code
    CDT
    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
    CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

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