BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

    AllTest Urinary Tract Infection Test

    K Number: K252607 · Decision Oct 30, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    12
    Applicant Total
    14
    Review Days
    73

    Basic Information

    Device Name
    AllTest Urinary Tract Infection Test
    K Number
    K252607
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1510
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Hangzhou AllTest Biotech Co., Ltd.
    Date Received
    August 18, 2025
    Decision Date
    October 30, 2025
    Product Code
    JMT
    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
    JMT Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)

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