Cordis Corp. - FDA 510(k) Cleared Devices

Cleared May 04, 2012

POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

K112797 · LIT

Cardiovascular · 221d

Cleared Jul 09, 2010

ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

K101651 · NTE

Cardiovascular · 28d

Cleared Aug 25, 2008

MICRO GUIDE CATHETER XP

K082143 · PDU

Cardiovascular · 26d

Cleared Apr 01, 2005

CORDIS AMIIA .014 PTA BALLOON CATHETER

K050645 · LIT

Cardiovascular · 18d

Cleared Dec 17, 2004

CORDIS STEER-IT DEFLECTING TIP GUIDEWIRE

K040592 · DQX

Cardiovascular · 284d

Cleared Oct 18, 2002

CORDIS OPTEASE PERMANENT VENA CAVA FILTER, MODELS 466-F200A, 466-F200B

K023116 · DTK

Cardiovascular · 29d

Cleared Jun 13, 2002

MODIFICATION TO ENVOY AND VISTA BRITE TIP

K021593 · DQY

Cardiovascular · 29d

Cleared Mar 20, 2002

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER WITH THE VISEASE ANGIOGRAPHIC...

K020316 · DQO

Cardiovascular · 49d

Cleared Jun 15, 2001

CORDIS M3 PTA DILATATION CATHETER

K003920 · DQY

Cardiovascular · 178d

Cleared Jun 06, 2001

TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT, MODEL 466-P306A

K010083 · DTK

Cardiovascular · 146d

Cleared Jan 19, 2001

TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND...

K003964 · DTK

Cardiovascular · 28d

Cleared Oct 30, 2000

CORDIS SLALOM PTA BALLOON CATHETER

K003159 · LIT

Cardiovascular · 20d