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

    SEEGENE ANYPLEX II HSV-1/2 ASSAY

    K Number: K142156 · Decision Feb 13, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    11
    Applicant Total
    1
    Review Days
    191

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    Basic Information

    Device Name
    SEEGENE ANYPLEX II HSV-1/2 ASSAY
    K Number
    K142156
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3305
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Seegene
    Date Received
    August 6, 2014
    Decision Date
    February 13, 2015
    Product Code
    OQO
    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
    OQO Herpes Simplex Virus Nucleic Acid Amplification Assay

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