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

    REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER

    K Number: K121913 · Decision Dec 20, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    19
    Registration Numbers
    19
    Same Product Code
    29
    Applicant Total
    2
    Review Days
    171

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    Basic Information

    Device Name
    REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER
    K Number
    K121913
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stryker Sustainability Solutions, Inc.
    Date Received
    July 2, 2012
    Decision Date
    December 20, 2012
    Product Code
    OWQ
    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
    OWQ Reprocessed Intravascular Ultrasound Catheter

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    Other Clearances by Stryker Sustainability Solutions, Inc.

    K Number Device Name
    K123334 REPROCESSED STEERABLE INTRODUCER