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

    SKIPPER AND SKIPPER RACE GUIDEWIRE

    K Number: K050756 · Decision May 5, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    258
    Same Product Code
    763
    Applicant Total
    7
    Review Days
    43

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    Basic Information

    Device Name
    SKIPPER AND SKIPPER RACE GUIDEWIRE
    K Number
    K050756
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Invatec Innovative Technologies, S.R.L.
    Date Received
    March 23, 2005
    Decision Date
    May 5, 2005
    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 Invatec Innovative Technologies, S.R.L.

    K Number Device Name
    K083919 AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER
    K052791 MODIFICATION TO: AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER
    K051917 DIVER C.E. CATHETER
    K050276 DIVER C.E. CATHETER
    K050073 MODIFICATION TO AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER
    K042624 AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER