BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Automated Insulin Dosing , Threshold Suspend

    PMA: P120010 · Supplement: S019 · Decision Jun 18, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18

    Basic Information

    Device Name
    Automated Insulin Dosing , Threshold Suspend
    Trade Name
    GLUCOSE SENSOR ENLITE
    PMA Number
    P120010
    Supplement Number
    S019
    Device Class
    FDA Class 3
    Product Code
    OZO
    Generic Name
    Automated insulin dosing , threshold suspend
    Medical Specialty
    Unknown
    Advisory Committee
    Clinical Chemistry
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    June 18, 2014
    Date Received
    March 21, 2014
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR CHANGES TO THE ENLITE GLUCOSE SENSOR (MMT-7008A, MMT-7008B) OF THE MINIMED 530G SYSTEM. SPECIFICALLY, THE SUPPLEMENT REQUESTED DESIGN MODIFICATIONS TO THE NEEDLE HUB AND NEEDLE CARRIER COMPONENTS OF THE ENLITE SENSOR TO FIT THE AUTOMATION MACHINE THAT WILL BE USED FOR THE SENSOR ASSEMBLY. ADDITIONALLY, THE NEW MANUFACTURING PROCESS WILL TAKE PLACE IN THE JUNCOS, PUERTO RICO MANUFACTURING SITE.

    Classifications

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

    Product Code Device Name
    OZO Automated Insulin Dosing , Threshold Suspend