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

    ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER

    K Number: K984189 · Decision May 5, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    26
    Review Days
    163

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    Basic Information

    Device Name
    ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER
    K Number
    K984189
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Maxxim Medical
    Date Received
    November 23, 1998
    Decision Date
    May 5, 1999
    Product Code
    FOZ
    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
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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