Cordis Europa, N.V.

7FDA 510(k) medical device clearances.

Top product codes for Cordis Europa, N.V.

FGE — Gastroenterology, Urology2 devices
KNQ — Gastroenterology, Urology2 devices
LIT — Cardiovascular2 devices
DQY — Cardiovascular1 device

Recent clearances by Cordis Europa, N.V.

K071189 — CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETERCode LIT·2007-05-16
K063563 — CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETERCode LIT·2007-03-07
K060302 — INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDEDCode KNQ·2006-04-11
K043605 — INSCOPE 3-STAGE BALLOON DILATORCode KNQ·2005-02-04
K040413 — CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEMCode FGE·2004-06-21
K032737 — CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTACode DQY·2003-10-02
K012056 — CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEMCode FGE·2001-08-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.