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

    DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.

    K Number: K800516 · Decision Mar 19, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    24
    Applicant Total
    253
    Review Days
    14

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    Basic Information

    Device Name
    DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.
    K Number
    K800516
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    E.I. Dupont DE Nemours & Co., Inc.
    Date Received
    March 5, 1980
    Decision Date
    March 19, 1980
    Product Code
    KIE
    Advisory Committee
    Clinical Chemistry
    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
    KIE Apparatus, High Pressure Liquid Chromatography

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