FDA 510(k) Applications Submitted by HEATHER MOROSE

FDA 510(k) Number Submission Date Device Name Applicant
K132673 08/27/2013 5F & 6F LAUNCHER GUIDE CATHETER, 5F SHERPA ACTIVE NX GUIDE CATHETER, 6F Z4 GUIDING CATHETER MEDTRONIC INC.
K103464 11/24/2010 PACIFIC XTREME PTCA BALLOON DILATATION CATHETER MEDTRONIC INC.


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