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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 10 Results
ProductCode: DWF Applicant: MEDTRONIC INC Decision Date To: 12/22/2014
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dlp silicone coronary artery ostial cann medtronic inc. K141951 08/15/2014
dlp retrograde coronary sinus perfusion medtronic inc. K132995 10/31/2013
dlp retrograde coronary sinus perfusion medtronic inc. K123762 03/27/2013
affinity fusion recirculation line model medtronic inc. K122913 10/19/2012
dlp single stage venous cannula, dlp rig medtronic inc. K120988 07/25/2012
dlp single stage venous cannula inflatab medtronic inc. K120987 06/06/2012
medtronic clear intravacular arteriotomy medtronic inc. K120612 05/25/2012
tubing, conmnectors, and accessories wit medtronic inc. K113845 01/25/2012
affinity cp centrifugal pump, resting he medtronic inc. K111972 07/27/2011
miar (minimally invasive aortic root) ca medtronic inc. K100274 05/10/2010
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