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

    HANSEN MEDICAL ARTISAN S CONTROL CATHETER

    K Number: K090365 · Decision May 7, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    32
    Applicant Total
    14
    Review Days
    83

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    Basic Information

    Device Name
    HANSEN MEDICAL ARTISAN S CONTROL CATHETER
    K Number
    K090365
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1290
    Medical Specialty
    Cardiovascular
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    Hansen Medical, Inc.
    Date Received
    February 13, 2009
    Decision Date
    May 7, 2009
    Product Code
    DXX
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXX System, Catheter Control, Steerable

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