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

    GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I

    K Number: K810043 · Decision May 15, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    2
    Applicant Total
    1
    Review Days
    128

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    Basic Information

    Device Name
    GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I
    K Number
    K810043
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3305
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Vibac Corp.
    Date Received
    January 7, 1981
    Decision Date
    May 15, 1981
    Product Code
    GQM
    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
    GQM Antisera, Neutralization, Herpesvirus Hominis

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