BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Venclose Maven™ Catheter

    Reg #: 3011879048 · FEI: 3011879048 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Venclose, Inc.
    Registration Number
    3011879048
    FEI Number
    3011879048
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2570 N 1st St Fl 2 # 221
    City
    San Jose
    State
    CA
    ZIP
    95131
    Country
    US

    Regulatory Submissions

    510(k) Number
    K211806

    Owner / Operator

    Firm Name
    C.R. Bard
    Operator Number
    10049916
    Address
    850 W Rio Salado Parkway
    City
    Tempe
    State
    AZ
    Postal Code
    85281
    Country
    US
    Correspondent
    Anisa Syed

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI

    Proprietary Names

    Venclose Maven™ Catheter VENCLOSE MAVEN™ Perforator RF Ablation Catheter Venclose Maven System (digiRF Generator and Maven Catheter) Venclose Power Cord Venclose Foot Pedal

    Establishment Types

    Manufacture Medical Device