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    FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

    ADVIA Centaur Herpes-2 IgG

    K Number: K181334 · Decision Aug 23, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    9
    Applicant Total
    23
    Review Days
    94

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    Basic Information

    Device Name
    ADVIA Centaur Herpes-2 IgG
    K Number
    K181334
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3305
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biokit, S.A.
    Date Received
    May 21, 2018
    Decision Date
    August 23, 2018
    Product Code
    MYF
    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
    MYF Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2

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    Other Clearances by Biokit, S.A.

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