BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Sensor, Glucose, Invasive

    PMA: P980022 · Supplement: S071 · Decision Oct 20, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23

    Basic Information

    Device Name
    Sensor, Glucose, Invasive
    Trade Name
    CONTINUOUS GLOCOSE MONITORING SYSTEM
    PMA Number
    P980022
    Supplement Number
    S071
    Device Class
    FDA Class 3
    Product Code
    MDS
    Generic Name
    Sensor, glucose, invasive
    Medical Specialty
    Unknown
    Advisory Committee
    Clinical Chemistry
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    October 20, 2011
    Date Received
    April 22, 2010
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR INCORPORATING A USB CONNECTION FOR DATA UPLOAD, CHANGING THE OPERATING TIME BEFORE RECHARGING, CHANGING TO A WEB-BASED SOFTWARE SYSTEM, AND INCORPORATING A DOCKING STATION AND CLEANING PLUG. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADENAME IPRO2 PROFESSIONAL CONTINUOUS GLUCOSE MONITORING (CGM) SYSTEM (MMT-7745).

    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