BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Rist 079 Radial Access Guide Catheter

    Reg #: 3015550451 · FEI: 3015550451 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR
    Registration Number
    3015550451
    FEI Number
    3015550451
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5290 California Avenue
    City
    Irvine
    State
    CA
    ZIP
    92617
    Country
    US

    Regulatory Submissions

    510(k) Number
    K241388

    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
    Catheter, Intravascular, Diagnostic DQO
    Catheter, Percutaneous, Neurovasculature QJP
    Catheter, Percutaneous DQY

    Proprietary Names

    Rist 079 Radial Access Guide Catheter Rist 071 Radial Access Guide Catheter Rist Radial Access Selective Catheter

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility