FDA 510(k) Applications Submitted by Colleen Mullins

FDA 510(k) Number Submission Date Device Name Applicant
K100470 02/18/2010 GTX 12 GIDEWIRE MEDTRONIC INC.
K130536 03/01/2013 EXPORT ADVANCE ASPIRATION CATHETER MEDTRONIC INC.
K101339 05/12/2010 ARCHER SUPER STIFF GUIDEWIRES MEDTRONIC INC.
K091582 06/02/2009 GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15 MEDTRONIC VASCULAR
K162027 07/22/2016 TRAcelet Compression Device MEDTRONIC VASCULAR
K152335 08/19/2015 Export Advance Aspiration Catheter Medtronic, Inc.
K192296 08/23/2019 Medtronic 6F Taiga Guiding Catheter Medtronic Vascular
K073523 12/14/2007 INTERCEPTOR PLUS CORONARY FILTER SYSTEMS MEDTRONIC INC.


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