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

    AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304

    K Number: K042623 · Decision Jan 27, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    273
    Registration Numbers
    273
    Same Product Code
    701
    Applicant Total
    2
    Review Days
    122

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    Basic Information

    Device Name
    AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304
    K Number
    K042623
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    St. Jude Medical, Daig Division, Inc.
    Date Received
    September 27, 2004
    Decision Date
    January 27, 2005
    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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