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

    PARKER AMBULATORY MEDICATION INFUSION PUMP 2004

    K Number: K897086 · Decision Sep 28, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    8
    Review Days
    282

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    Basic Information

    Device Name
    PARKER AMBULATORY MEDICATION INFUSION PUMP 2004
    K Number
    K897086
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Parker Hannifin Corp.
    Date Received
    December 20, 1989
    Decision Date
    September 28, 1990
    Product Code
    FRN
    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
    FRN Pump, Infusion

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