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

    VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG

    K Number: K903882 · Decision Dec 4, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    9
    Applicant Total
    6
    Review Days
    104

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    Basic Information

    Device Name
    VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG
    K Number
    K903882
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3900
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Viral Antigens, Inc.
    Date Received
    August 22, 1990
    Decision Date
    December 4, 1990
    Product Code
    GQW
    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
    GQW Antigen, Cf, (Including Cf Control), Varicella-Zoster

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    Other Clearances by Viral Antigens, Inc.

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