BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

    GENTLECATH MALE COUDE OLIVE TIP INTERMITTENT URINARY CATHETER

    K Number: K140953 · Decision Aug 1, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    114
    Registration Numbers
    114
    Same Product Code
    237
    Applicant Total
    4
    Review Days
    109

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    Basic Information

    Device Name
    GENTLECATH MALE COUDE OLIVE TIP INTERMITTENT URINARY CATHETER
    K Number
    K140953
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5130
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Convatec, Ltd.
    Date Received
    April 14, 2014
    Decision Date
    August 1, 2014
    Product Code
    KOD
    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
    KOD Catheter, Urological

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