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

    DETECTOR, MODEL 79875A, VARIABLE

    K Number: K781771 · Decision Dec 20, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    24
    Applicant Total
    230
    Review Days
    68

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    Basic Information

    Device Name
    DETECTOR, MODEL 79875A, VARIABLE
    K Number
    K781771
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Hewlett-Packard Co.
    Date Received
    October 13, 1978
    Decision Date
    December 20, 1978
    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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