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

    L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters

    K Number: K230669 · Decision Nov 30, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    301
    Applicant Total
    5
    Review Days
    265

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    Basic Information

    Device Name
    L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters
    K Number
    K230669
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5970
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Argon Medical Devices
    Date Received
    March 10, 2023
    Decision Date
    November 30, 2023
    Product Code
    LJS
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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