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

    INDIRECT FLUORESCENT ASSAY FOR (HCMV)

    K Number: K882835 · Decision Dec 5, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    18
    Applicant Total
    7
    Review Days
    150

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    Basic Information

    Device Name
    INDIRECT FLUORESCENT ASSAY FOR (HCMV)
    K Number
    K882835
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3175
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Stellar Bio Systems, Inc.
    Date Received
    July 8, 1988
    Decision Date
    December 5, 1988
    Product Code
    GQH
    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
    GQH Antigen, Cf (Including Cf Control), Cytomegalovirus

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