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

    OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER

    K Number: K091077 · Decision Feb 4, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    82
    Applicant Total
    5
    Review Days
    296

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    Basic Information

    Device Name
    OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER
    K Number
    K091077
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.3375
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Cordis Corp., A Johnson & Johnson Co.
    Date Received
    April 14, 2009
    Decision Date
    February 4, 2010
    Product Code
    DTK
    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
    DTK Filter, Intravascular, Cardiovascular

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