BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DxC 500i Clinical Analyzer, DxC 500i AU Chemistry Module, C63522

    Reg #: 2122870 · FEI: 2122870 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BECKMAN COULTER, INC.
    Registration Number
    2122870
    FEI Number
    2122870
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1000 LAKE HAZELTINE DR.
    City
    CHASKA
    State
    MN
    ZIP
    55318
    Country
    US

    Regulatory Submissions

    510(k) Number
    K242190

    Owner / Operator

    Firm Name
    BECKMAN COULTER, INC.
    Operator Number
    2050012
    Address
    250 S. Kraemer Blvd, --
    City
    Brea
    State
    CA
    Postal Code
    92821
    Country
    US
    Correspondent
    David G Davis

    Products

    Device Name Product Code
    Analyzer, Chemistry (Photometric, Discrete), For Clinical Use JJE

    Proprietary Names

    DxC 500i Clinical Analyzer, DxC 500i AU Chemistry Module, C63522 DxC 500i Clinical Analyzer, DxC 500i Access 2 Immunoassay Module, C13252 DxC 500i Clinical Analyzer, DxC 500i AU Chemistry Module, C63521

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)