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

    WATERS 717 AUTOSAMPLER

    K Number: K920136 · Decision Feb 19, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    18
    Applicant Total
    30
    Review Days
    37

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    Basic Information

    Device Name
    WATERS 717 AUTOSAMPLER
    K Number
    K920136
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Millipore Corp.
    Date Received
    January 13, 1992
    Decision Date
    February 19, 1992
    Product Code
    LDM
    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
    LDM Instrumentation, High Pressure Liquid Chromatography

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