FDA 510(k) Applications Submitted by KAREN JONES

FDA 510(k) Number Submission Date Device Name Applicant
K120072 01/10/2012 VENOUS DRAINAGE CANNULA WITH DURAFLO COATING EDWARDS LIFESCIENCES, LLC.
K092509 08/17/2009 EDWARDS LIFESCIENCES VENOUS RETURN CANNULAE EDWARDS LIFESCIENCES, LLC.
K002578 08/18/2000 AXILLARY ACCESS ARTERIAL CANNULA EDWARDS LIFESCIENCES, LLC.
K062429 08/21/2006 MODIFICATION TO EMBOL-X INTRA-AORTIC FILTER: X-SMALL, SMALL, MEDIUM, LARGE, X-LARGE WITH HEPARIN COATED MESH EDWARDS LIFESCIENCES RESEARCH MEDICAL
K123187 10/11/2012 RETROGRADE CORONARY SINUS CARDIOPLEGIA CATHETER, RETROGRADE CARDIOPLEGIA CATHETER, RETROGRADE CARDIOPLEGIA CANNULA EDWARDS LIFESCIENCES, LLC.
K123370 11/01/2012 EZ GLIDE AORTIC CANNULA, AORTIC PERFUSION CANNULA WITH DURAFLO COATING, DISPERSION AORTIC PERFUSION CANNULA EDWARDS LIFESCIENCES, LLC.
K113667 12/13/2011 CARDIOPLEGIA DELIVERY SETS CARDIOPLEGIA DELIVERY SETS WITH DURAFLO COATING EDWARDS LIFESCIENCES, LLC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact