BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MILLIPORE DUAL RATE INTRAVENOUS CASSETTE

    K Number: K811432 · Decision Jul 13, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    59
    Applicant Total
    30
    Review Days
    52

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    Basic Information

    Device Name
    MILLIPORE DUAL RATE INTRAVENOUS CASSETTE
    K Number
    K811432
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Millipore Corp.
    Date Received
    May 22, 1981
    Decision Date
    July 13, 1981
    Product Code
    LDR
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LDR Controller, Infusion, Intravascular, Electronic

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