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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 11 Results
ProductCode: DQY Applicant: MEDTRONIC INC. Decision Date To: 03/28/2024
 
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510(K)
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5f & 6f launcher guide catheter, 5f sherpa active nx guide catheter, 6f z4 guiding catheter MEDTRONIC INC. K132673 10/22/2013
attain clarity 6225 venogram balloon catheter MEDTRONIC INC. K121219 09/25/2012
attain command 6250 left heart delivery systems and attain command 6250 guide catheters for left heart delivery MEDTRONIC INC. K080428 12/09/2008
attain command 6250 left heart delivery systems and guide catheters for left heart delivery MEDTRONIC INC. K090659 03/26/2009
medtronic c315 delivery catheter MEDTRONIC INC. K101885 09/09/2010
medtronic selectsite deflectable catheter system, models c304-s59 and c304-l69 MEDTRONIC INC. CARDIAC RHYTHM MANAGEMENT K033989 01/22/2004
medtronic vascular - hub material modification to the 5f and 8f launcher(r) guide catheters MEDTRONIC INC. K103386 02/11/2011
modification to: attain prevail 6228cth80 steerable catheter set MEDTRONIC INC. K082670 12/04/2008
pacific xtreme ptca balloon dilatation catheter MEDTRONIC INC. K103464 12/22/2010
selectsite c304-his deflectable catheter system Medtronic Inc. K183493 03/15/2019
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