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

    PROCAINAMIDE ANALYTICAL TEST PACK

    K Number: K833384 · Decision Dec 27, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    24
    Applicant Total
    253
    Review Days
    89

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    Basic Information

    Device Name
    PROCAINAMIDE ANALYTICAL TEST PACK
    K Number
    K833384
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3320
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Applicant
    E.I. Dupont DE Nemours & Co., Inc.
    Date Received
    September 29, 1983
    Decision Date
    December 27, 1983
    Product Code
    LAR
    Advisory Committee
    Clinical Toxicology
    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
    LAR Enzyme Immunoassay, Procainamide

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