BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    FIRST RESPONSE GOLD DIGITAL PREGNANCY TEST

    K Number: K123567 · Decision Sep 10, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    225
    Applicant Total
    29
    Review Days
    294

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    Basic Information

    Device Name
    FIRST RESPONSE GOLD DIGITAL PREGNANCY TEST
    K Number
    K123567
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Church & Dwight Co., Inc.
    Date Received
    November 20, 2012
    Decision Date
    September 10, 2013
    Product Code
    LCX
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

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

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