BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VITEK REVEAL BC GN02-AST

    Reg #: 2919016 · FEI: 2919016 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Beckman Coulter, Inc.
    Registration Number
    2919016
    FEI Number
    2919016
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2040 ENTERPRISE BLVD.
    City
    West Sacramento
    State
    CA
    ZIP
    95691
    Country
    US

    Regulatory Submissions

    510(k) Number
    K230675

    Owner / Operator

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

    Products

    Device Name Product Code
    Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples SAN
    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation LON

    Proprietary Names

    VITEK REVEAL BC GN02-AST

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)