BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Spectrum Central Venous Tray Double Lumen Polyurethane Catheter Minocycline/Rifampin Impregnated

    Reg #: 1820334 · FEI: 1820334 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    Cook Incorporated
    Registration Number
    1820334
    FEI Number
    1820334
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    750 DANIELS WAY
    City
    Bloomington
    State
    IN
    ZIP
    47404
    Country
    US

    Regulatory Submissions

    510(k) Number
    K021557

    Owner / Operator

    Firm Name
    COOK, INC.
    Operator Number
    1820334
    Address
    750 DANIELS WAY
    City
    Bloomington
    State
    IN
    Postal Code
    47404
    Country
    US

    Products

    Device Name Product Code
    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days FOZ
    Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days LJS

    Proprietary Names

    Spectrum Central Venous Tray Double Lumen Polyurethane Catheter Minocycline/Rifampin Impregnated Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Double Lumen Polyurethane Catheter

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device