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

    FTA-ABS TEST

    K Number: K801959 · Decision Oct 23, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    3
    Applicant Total
    8
    Review Days
    65

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    Basic Information

    Device Name
    FTA-ABS TEST
    K Number
    K801959
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3830
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Immuno-Diagnostic Products, Inc.
    Date Received
    August 19, 1980
    Decision Date
    October 23, 1980
    Product Code
    JWL
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JWL Antigen, Treponema Pallidum For Fta-Abs Test

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