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

    ATW MARKER WIRE STEERABLE GUIDEWIRE

    K Number: K994358 · Decision Jan 13, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    258
    Same Product Code
    763
    Applicant Total
    315
    Review Days
    17

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    Basic Information

    Device Name
    ATW MARKER WIRE STEERABLE GUIDEWIRE
    K Number
    K994358
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Cordis Corp.
    Date Received
    December 27, 1999
    Decision Date
    January 13, 2000
    Product Code
    DQX
    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
    DQX Wire, Guide, Catheter

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