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

    MD2 PERSONAL INFUSION SYSTEM

    K Number: K896544 · Decision May 2, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    20
    Review Days
    166

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    Basic Information

    Device Name
    MD2 PERSONAL INFUSION SYSTEM
    K Number
    K896544
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Norfolk Medical Products, Inc.
    Date Received
    November 17, 1989
    Decision Date
    May 2, 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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