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

    MAX L SYSTEM

    K Number: K761168 · Decision Dec 10, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    15
    Applicant Total
    1
    Review Days
    9

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    Basic Information

    Device Name
    MAX L SYSTEM
    K Number
    K761168
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Brinkman Instruments, Inc.
    Date Received
    December 1, 1976
    Decision Date
    December 10, 1976
    Product Code
    DPM
    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
    DPM Columns, Liquid Chromatography

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