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

    Sensor, Glucose, Invasive

    PMA: P980022 · Supplement: S157 · Decision Jul 18, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23

    Basic Information

    Device Name
    Sensor, Glucose, Invasive
    Trade Name
    MYSENTRY SYSTEM, MYSENTRY MONITOR, MYSENTRY OUTPOST
    PMA Number
    P980022
    Supplement Number
    S157
    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
    July 18, 2014
    Date Received
    June 18, 2014
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    ADDITION OF A FUNCTIONAL TEST DURING MANUFACTURE OF THE MYSENTRY SYSTEM (MMT-9100). THE MYSENTRY SYSTEM (MMT-9100) CONSISTS OF THE MYSENTRY MONITOR (MMT-9101) AND MYSENTRY OUTPOST (MMT-9102) AND IS APPROVED FOR USE WITH THE PARADIGM REALTIME 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