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

    UNITIP HIGH RESOLUTION CATHETER

    K Number: K062222 · Decision Mar 15, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    68
    Applicant Total
    2
    Review Days
    225

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    Basic Information

    Device Name
    UNITIP HIGH RESOLUTION CATHETER
    K Number
    K062222
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1725
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Unisensor AG
    Date Received
    August 2, 2006
    Decision Date
    March 15, 2007
    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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    Other Clearances by Unisensor AG

    K Number Device Name
    K003580 UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETER