BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LINQ Tool Kit

    Reg #: 3004185781 · FEI: 3004185781 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic, Inc.
    Registration Number
    3004185781
    FEI Number
    3004185781
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2343 W. Medtronic Way
    City
    Tempe
    State
    AZ
    ZIP
    85281
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200795

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    Products

    Device Name Product Code
    Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection) MXD

    Proprietary Names

    LINQ Tool Kit LINQ II Insertable Cardiac Monitor

    Establishment Types

    Manufacture Medical Device