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

    DETERMINATION OF QUINIDINE

    K Number: K860049 · Decision Jan 22, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    26
    Applicant Total
    36
    Review Days
    16

    Basic Information

    Device Name
    DETERMINATION OF QUINIDINE
    K Number
    K860049
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3320
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Applicant
    CLINICAL DATA, INC.
    Date Received
    January 6, 1986
    Decision Date
    January 22, 1986
    Product Code
    LBZ
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LBZ Enzyme Immunoassay, Quinidine

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