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

    Sensor, Glucose, Invasive

    PMA: P980022 · Supplement: S202 · Decision Feb 28, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23

    Basic Information

    Device Name
    Sensor, Glucose, Invasive
    Trade Name
    Paradigm real time Insulin Pump / Paradigm Real time revel Insulin Pump
    PMA Number
    P980022
    Supplement Number
    S202
    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
    February 28, 2018
    Date Received
    January 29, 2018
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    Change of O-ring supplier for MiniMed 630G, 670G, and Paradigm REAL-Time family of insulin pumps, which are components of the MiniMed 670G System, MiniMed 630G System with SmartGuard, MiniMed Paradigm Real-Time Revel System with Enlite Sensor, MiniMed 530G System, and MiniMed Paradigm Real-Time Revel System.

    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