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

    CATHETER, FEMORAL VEIN, SF 6

    K Number: K772148 · Decision Nov 29, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    4
    Applicant Total
    69
    Review Days
    15

    Basic Information

    Device Name
    CATHETER, FEMORAL VEIN, SF 6
    K Number
    K772148
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    SORENSEN RESEARCH
    Date Received
    November 14, 1977
    Decision Date
    November 29, 1977
    Product Code
    FJT
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    HE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FJT Intracatheter, Dialysis

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