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

    INSTANT-VIEW FECAL OCCULT BLOOD RAPID TEST

    K Number: K021423 · Decision Jun 17, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    96
    Applicant Total
    43
    Review Days
    45

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    Basic Information

    Device Name
    INSTANT-VIEW FECAL OCCULT BLOOD RAPID TEST
    K Number
    K021423
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    864.6550
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Alfa Scientific Designs, Inc.
    Date Received
    May 3, 2002
    Decision Date
    June 17, 2002
    Product Code
    KHE
    Advisory Committee
    Hematology
    Review Advisory Committee
    HE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KHE Reagent, Occult Blood

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