BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    KENLOR H. PYLORI CONTROL SERUM

    K Number: K964014 · Decision Mar 3, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    53
    Registration Numbers
    53
    Same Product Code
    90
    Applicant Total
    9
    Review Days
    147

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    Basic Information

    Device Name
    KENLOR H. PYLORI CONTROL SERUM
    K Number
    K964014
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.3110
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kenlor Industries, Inc.
    Date Received
    October 7, 1996
    Decision Date
    March 3, 1997
    Product Code
    LYR
    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
    LYR Helicobacter Pylori

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