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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.
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