FDA 510(k) Applications Submitted by EV3 CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K031864 06/16/2003 NITREX NITINOL GUIDEWIRE EV3 CORPORATION
K050725 03/21/2005 PROTEGE GPS SELF-EXPANDING NITINOL STENT EV3 CORPORATION
K051379 05/27/2005 PROTEGE RX GPS SELF-EXPANDING NITRINOL STENT EV3 CORPORATION
K021096 04/04/2002 X-SIZER CATHETER SYSTEM EV3 CORPORATION
K024021 12/05/2002 NITREX NITINOL GUIDEWIRE EV3 CORPORATION


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