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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 14 Results
ProductCode: DWF Applicant: EDWARDS LIFESCIENCES, LLC Decision Date To: 07/22/2014
 
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ferm-flex and fem-flex ii ( femoral acce edwards lifesciences, llc. K140208 03/05/2014
femoral access venous cannulae edwards lifesciences, llc. K123303 03/22/2013
fem-felx, fex-flex ii femoral access can edwards lifesciences, llc. K123298 03/15/2013
ez glide aortic cannula, aortic perfusio edwards lifesciences, llc. K123370 03/13/2013
retrograde coronary sinus cardioplegia c edwards lifesciences, llc. K123187 02/22/2013
anteplegia catheter antegrade cardiopleg edwards lifesciences, llc. K113459 06/29/2012
edward proplege peripheral retrograde ca edwards lifesciences, llc. K120780 06/27/2012
edward vent catheters edward vent cathet edwards lifesciences, llc. K113411 06/11/2012
venous drainage cannula with duraflo coa edwards lifesciences, llc. K120072 05/08/2012
embol-x access device/ aortic cannula, e edwards lifesciences, llc. K102420 10/26/2010
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