BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    hCG Urine Test Strip, hCG Urine Test Cassette, hCG Urine Test Midstream

    K Number: K200133 · Decision Aug 13, 2020
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    225
    Applicant Total
    9
    Review Days
    205

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    Basic Information

    Device Name
    hCG Urine Test Strip, hCG Urine Test Cassette, hCG Urine Test Midstream
    K Number
    K200133
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Safecare Biotech (Hangzhou) Co., Ltd.
    Date Received
    January 21, 2020
    Decision Date
    August 13, 2020
    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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