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

    SYRINGE INFUSION PUMP

    K Number: K791729 · Decision Oct 1, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    2
    Review Days
    32

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    Basic Information

    Device Name
    SYRINGE INFUSION PUMP
    K Number
    K791729
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Princeton Medical Instruments, Inc.
    Date Received
    August 30, 1979
    Decision Date
    October 1, 1979
    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 Princeton Medical Instruments, Inc.

    K Number Device Name
    K802400 MS 16 SYRINGE DRIVER