Cordis Europa, N.V.
Cordis Europa, N.V. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2007.
Top product codes for Cordis Europa, N.V.
Recent clearances by Cordis Europa, N.V.
- K071189 — CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER
- K063563 — CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER
- K060302 — INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
- K043605 — INSCOPE 3-STAGE BALLOON DILATOR
- K040413 — CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM
- K032737 — CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA
- K012056 — CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.