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

    CONVEY 7F GUIDING CATHETER, CONVEY 8F GUIDING CATHETER

    K Number: K132197 · Decision Aug 12, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    277
    Same Product Code
    889
    Applicant Total
    2
    Review Days
    27

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    Basic Information

    Device Name
    CONVEY 7F GUIDING CATHETER, CONVEY 8F GUIDING CATHETER
    K Number
    K132197
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pendracare International, B.V.
    Date Received
    July 16, 2013
    Decision Date
    August 12, 2013
    Product Code
    DQY
    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
    DQY Catheter, Percutaneous

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    Other Clearances by Pendracare International, B.V.

    K Number Device Name
    K120585 CONVEY GUIDING CATHETER