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

    XPECT INFLUENZA A/B

    K Number: K031565 · Decision Jul 17, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    36
    Registration Numbers
    36
    Same Product Code
    71
    Applicant Total
    17
    Review Days
    59

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    Basic Information

    Device Name
    XPECT INFLUENZA A/B
    K Number
    K031565
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3328
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Remel, Inc.
    Date Received
    May 19, 2003
    Decision Date
    July 17, 2003
    Product Code
    PSZ
    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
    PSZ Devices Detecting Influenza A, B, And C Virus Antigens

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