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

    CMV BRITE TURBO KIT

    K Number: K991650 · Decision Jul 12, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    16
    Applicant Total
    5
    Review Days
    60

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    Basic Information

    Device Name
    CMV BRITE TURBO KIT
    K Number
    K991650
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    866.3175
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biotest Diagnostics Corp.
    Date Received
    May 13, 1999
    Decision Date
    July 12, 1999
    Product Code
    LIN
    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
    LIN Antisera, Conjugated Fluorescent, Cytomegalovirus

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