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

    MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE

    K Number: K903647 · Decision Sep 11, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    18
    Applicant Total
    30
    Review Days
    33

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    Basic Information

    Device Name
    MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE
    K Number
    K903647
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Millipore Corp.
    Date Received
    August 9, 1990
    Decision Date
    September 11, 1990
    Product Code
    LDM
    Advisory Committee
    Clinical Chemistry
    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
    LDM Instrumentation, High Pressure Liquid Chromatography

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