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

    PILOT CARDIOVASCULAR SYSTEMS 2 CM PILOT WIRE

    K Number: K934474 · Decision Nov 8, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    258
    Same Product Code
    763
    Applicant Total
    2
    Review Days
    55

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    Basic Information

    Device Name
    PILOT CARDIOVASCULAR SYSTEMS 2 CM PILOT WIRE
    K Number
    K934474
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard
    Date Received
    September 14, 1993
    Decision Date
    November 8, 1993
    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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    Other Clearances by Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard

    K Number Device Name
    K924009 INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE