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

    PROGRAMED

    K Number: K832349 · Decision Nov 28, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    2
    Review Days
    133

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    Basic Information

    Device Name
    PROGRAMED
    K Number
    K832349
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Intrabionic Co.
    Date Received
    July 18, 1983
    Decision Date
    November 28, 1983
    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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    Other Clearances by Intrabionic Co.

    K Number Device Name
    K832350 INTRABIONIC CO. - MICRO SYRINGE