BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

    URINALYSIS REAGENT STRIPS (10 PARAMETERS)

    K Number: K993850 · Decision Jan 3, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    12
    Applicant Total
    8
    Review Days
    52

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    Basic Information

    Device Name
    URINALYSIS REAGENT STRIPS (10 PARAMETERS)
    K Number
    K993850
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1510
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    International Newtech Development, Inc.
    Date Received
    November 12, 1999
    Decision Date
    January 3, 2000
    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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    K951705 MINISTRIP HCG