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

    GUIDE WIRE BOWL

    K Number: K873942 · Decision Dec 23, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    258
    Same Product Code
    763
    Applicant Total
    3
    Review Days
    86

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    Basic Information

    Device Name
    GUIDE WIRE BOWL
    K Number
    K873942
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Condor Medical
    Date Received
    September 28, 1987
    Decision Date
    December 23, 1987
    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 Condor Medical

    K Number Device Name
    K873985 FLUORO COVER
    K873709 3 RING ATTACHMENT FOR SYRINGES