BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

    Reg #: 3005402529 · FEI: 3005402529 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ACCESS POINT TECHNOLOGIES, EP INC.
    Registration Number
    3005402529
    FEI Number
    3005402529
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    12560 FLETCHER LANE, SUITE 300
    City
    Rogers
    State
    MN
    ZIP
    55374
    Country
    US

    Owner / Operator

    Firm Name
    Stereotaxis
    Operator Number
    9048165
    Address
    710 N. Tucker Blvd., Suite 110
    City
    Saint Louis
    State
    MO
    Postal Code
    63101
    Country
    US
    Correspondent
    Angela McKnight

    Products

    Device Name Product Code
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE

    Proprietary Names

    Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

    Establishment Types

    Manufacture Device in the United States for Export Only