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

    TELEFLEX STEERABLE GUIDEWIRE

    K Number: K871850 · Decision Jan 27, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    258
    Same Product Code
    763
    Applicant Total
    64
    Review Days
    260

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    Basic Information

    Device Name
    TELEFLEX STEERABLE GUIDEWIRE
    K Number
    K871850
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Teleflexmedical, Inc.
    Date Received
    May 12, 1987
    Decision Date
    January 27, 1988
    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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