BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Pulse Generator, Permanent, Implantable

    PMA: P890003 · Supplement: S095 · Decision Nov 22, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35

    Basic Information

    Device Name
    Pulse Generator, Permanent, Implantable
    Trade Name
    MEDTRONIC REVEAL PLUS INSERTABLE LOOP RECORDER (ILR) APPLICATION SOFTWARE MODEL 9809
    PMA Number
    P890003
    Supplement Number
    S095
    Device Class
    FDA Class 3
    Product Code
    NVZ
    Generic Name
    Pulse generator, permanent, implantable
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    November 22, 2005
    Date Received
    October 19, 2005
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A SOFTWARE UPDATE, SOFTWARE SERIES 5.0 TO SOFTWARE SERIES 6.0, TO CORRECT A MINOR CUSTOMER INCONVENIENCE ANOMALY WITH TELEMETRY ERROR CONDITIONS RELATED TO THE RETRY STRATEGY BY ADDITION OF AN ENHANCEMENT CHECK TO ENSURE THAT ALL OF THE EVENT DATA HAS BEEN RECEIVED.

    Classifications

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

    Product Code Device Name
    NVZ Pulse Generator, Permanent, Implantable