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

    Mini Stick ENVI Non-Vascular Introducer Kit

    K Number: K170775 · Decision Jul 19, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    273
    Registration Numbers
    273
    Same Product Code
    701
    Applicant Total
    87
    Review Days
    127

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    Basic Information

    Device Name
    Mini Stick ENVI Non-Vascular Introducer Kit
    K Number
    K170775
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    AngioDynamics, Inc.
    Date Received
    March 14, 2017
    Decision Date
    July 19, 2017
    Product Code
    DYB
    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
    DYB Introducer, Catheter

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