BEUDAMED
    FDA Registration Active 🇺🇸 United States

    First Response Rapid Result Pregnancy Test

    Reg #: 2280705 · FEI: 2280705 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    CHURCH & DWIGHT CO., INC.
    Registration Number
    2280705
    FEI Number
    2280705
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    469 NORTH HARRISON STREET
    City
    PRINCETON
    State
    NJ
    ZIP
    08543
    Country
    US

    Regulatory Submissions

    510(k) Number
    K973352

    Owner / Operator

    Firm Name
    CHURCH & DWIGHT CO., INC.
    Operator Number
    2210299
    Address
    500 Charles Ewing Blvd., --
    City
    Ewing Township
    State
    NJ
    Postal Code
    08628
    Country
    US

    Products

    Device Name Product Code
    Kit, Test, Pregnancy, Hcg, Over The Counter LCX

    Proprietary Names

    First Response Rapid Result Pregnancy Test First Response Pregnancy Triple Check Pregnancy Test Kit First Response™ Multi Check Convenience Kit Pregnancy Test Kit

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198