BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Xcess Guiding Catheter

    Reg #: 3008361782 · FEI: 3008361782 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Curatia Medical Co.
    Registration Number
    3008361782
    FEI Number
    3008361782
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    830 Stewart Drive
    City
    Sunnyvale
    State
    CA
    ZIP
    94085
    Country
    US

    Regulatory Submissions

    510(k) Number
    K180797

    Owner / Operator

    Firm Name
    Curatia Medical Co.
    Operator Number
    10031704
    Address
    830 Stewart Drive
    City
    Sunnyvale
    State
    CA
    Postal Code
    94085
    Country
    US
    Correspondent
    Jessica Chiu

    Products

    Device Name Product Code
    Catheter, Percutaneous DQY

    Proprietary Names

    Xcess Guiding Catheter

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility