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

    Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)

    K Number: K241028 · Decision Jul 26, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    86
    Registration Numbers
    86
    Same Product Code
    81
    Applicant Total
    15
    Review Days
    102

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    Basic Information

    Device Name
    Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)
    K Number
    K241028
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5130
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Coloplast
    Date Received
    April 15, 2024
    Decision Date
    July 26, 2024
    Product Code
    EZD
    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
    EZD Catheter, Straight

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