FDA 510(k) Applications Submitted by CORDIS EUROPA N.V.

FDA 510(k) Number Submission Date Device Name Applicant
K012056 07/02/2001 CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM CORDIS EUROPA N.V.
K040413 02/18/2004 CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM CORDIS EUROPA N.V.
K032737 09/04/2003 CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA CORDIS EUROPA N.V.


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