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

    INSIGHT SPHINCTER OF ODDI MANOMETRY MODULE, MODEL S981300

    K Number: K990441 · Decision May 12, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    68
    Applicant Total
    16
    Review Days
    90

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    Basic Information

    Device Name
    INSIGHT SPHINCTER OF ODDI MANOMETRY MODULE, MODEL S981300
    K Number
    K990441
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1725
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sandhill Scientific, Inc.
    Date Received
    February 11, 1999
    Decision Date
    May 12, 1999
    Product Code
    FFX
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FFX System, Gastrointestinal Motility (Electrical)

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