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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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