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

    AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER

    K Number: K131814 · Decision Jul 26, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    123
    Applicant Total
    6
    Review Days
    36

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    Basic Information

    Device Name
    AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER
    K Number
    K131814
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    876.5540
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Ameco Medical Industries
    Date Received
    June 20, 2013
    Decision Date
    July 26, 2013
    Product Code
    MSD
    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
    MSD Catheter, Hemodialysis, Implanted

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    Other Clearances by Ameco Medical Industries

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    K110794 AMECATH CVC AND AMECATH PRESSURE CVC SHORT TERM SINGLE AND MULTI-LUMEN CATHERIZATION KITS
    K110793 AMECATH AND AMECATH UNIQATH SOFT SHORT TERM DUAL HEMODIALYSIS CATHETERIZATION KITS