BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Sensor, Glucose, Invasive

    PMA: P980022 · Supplement: S148 · Decision Dec 5, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23

    Basic Information

    Device Name
    Sensor, Glucose, Invasive
    Trade Name
    PARADIGM REAL-TIME SYSTEM, PARADIGM REAL-TIME REVEL SYSTEM AND GUARDIAN REAL-TIME CGM SYSTEM
    PMA Number
    P980022
    Supplement Number
    S148
    Device Class
    FDA Class 3
    Product Code
    MDS
    Generic Name
    Sensor, glucose, invasive
    Medical Specialty
    Unknown
    Advisory Committee
    Clinical Chemistry
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    December 5, 2013
    Date Received
    November 8, 2013
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    PC-BASED MANUFACTURING SOFTWARE UPDATE FROM VERSION 2.2A TO VERSION 2.3A AT THE MEDTRONIC MINIMED, NORTHRIDGE FACILITY, AND UPDATE FROM VERSION 2.0D TO VERSION 2.3A AT THE MPROC, JUNCOS FACILITY FOR THE PARADIGM REAL-TIME INSULIN PUMP (MODELS: MMT-522, MMT-522K, MMT-722, AND MMT-722K), THE PARADIGM REAL-TIME REVEL INSULIN PUMP (MODELS: MMT-523, MMT-523K, MMT-723, AND MMT-723K), THE GUARDIAN REAL-TIME MONITOR (MODEL: CSS7100) AND THE MINIMED 530G INSULIN PUMP (MODELS MMT-551 AND MMT-751).

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MDS Sensor, Glucose, Invasive