BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Aquatrack Hydrophilic Nitinol Guidewire

    Reg #: 3007635982 · FEI: 3007635982 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Confluent Medical Technologies, Inc
    Registration Number
    3007635982
    FEI Number
    3007635982
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    47533 Westinghouse Dr
    City
    Fremont
    State
    CA
    ZIP
    94539
    Country
    US

    Regulatory Submissions

    510(k) Number
    K011905

    Owner / Operator

    Firm Name
    Confluent Medical Technologies, Inc.
    Operator Number
    10033958
    Address
    6263 N. Scottsdale Road, Suite 224
    City
    Scottsdale
    State
    AZ
    Postal Code
    85250
    Country
    US
    Correspondent
    Rich Brown

    Products

    Device Name Product Code
    Wire, Guide, Catheter DQX

    Proprietary Names

    Aquatrack Hydrophilic Nitinol Guidewire

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility