BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    APPLELISA CHLAMYDIA TRACHOMATIS ANTI

    K Number: K843120 · Decision Sep 12, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    66
    Applicant Total
    7
    Review Days
    35

    Basic Information

    Device Name
    APPLELISA CHLAMYDIA TRACHOMATIS ANTI
    K Number
    K843120
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.3120
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    APPLE DIAGNOSTIC PRODUCTS
    Date Received
    August 8, 1984
    Decision Date
    September 12, 1984
    Product Code
    LJC
    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
    LJC Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)

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