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News Daily News

FDA: Class 1 Recall for Boston Scientific’s RotaWire Elite, WireClip Torquer Guidewires

Shelley Wood

November 29, 2015

News Daily News

Good News, Bad News Week for Watchman LAA Occluder

Shelley Wood

November 12, 2015

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

News Daily News

Liliana Grinfeld, Pioneering Interventional Cardiologist From Argentina, Dies at 71

L.A. McKeown

June 01, 2015

News Industry News

Vascular Solutions, Inc. Issues Recall of Langston® Dual Lumen Catheters

July 03, 2014

News Industry News

Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

May 12, 2014

News Daily News

Cardiovascular Devices Make Up Largest Class of FDA Device Recalls Since 2005

Yael L. Maxwell

April 03, 2014

News Daily News

Drug-Eluting Balloons Reduce Restenosis, TLR in Diabetic Patients with CLI

Yael L. Maxwell

February 26, 2014

News Daily News

Debate: PCI vs. CABG for Left Main Disease

November 07, 2011

News Daily News

Xience Shows Noninferior Late Loss to Cypher, Similar Hard Outcomes

October 17, 2011

News Daily News

NEJM Articles Argue to Sack FDA’s Device Clearance Process

Caitlin E. Cox

August 12, 2011

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

Caitlin E. Cox

July 20, 2011

News Industry News

Boston Scientific Announces Voluntary Recall of iCross™ Coronary Imaging Catheters

May 27, 2011

News Daily News

Report on Device Recalls Criticizes Current FDA Approval Process

L.A. McKeown

February 14, 2011

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FDA: Class 1 Recall for Boston Scientific’s RotaWire Elite, WireClip Torquer Guidewires

Good News, Bad News Week for Watchman LAA Occluder

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Liliana Grinfeld, Pioneering Interventional Cardiologist From Argentina, Dies at 71

Vascular Solutions, Inc. Issues Recall of Langston® Dual Lumen Catheters

Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

Cardiovascular Devices Make Up Largest Class of FDA Device Recalls Since 2005

Drug-Eluting Balloons Reduce Restenosis, TLR in Diabetic Patients with CLI

More Than Half of Readmissions Within 30 Days of Acute MI Unrelated to Index Event

Debate: PCI vs. CABG for Left Main Disease

Xience Shows Noninferior Late Loss to Cypher, Similar Hard Outcomes

NEJM Articles Argue to Sack FDA’s Device Clearance Process

Commentary Authors Urge Improvements to Device Approval Process

Boston Scientific Announces Voluntary Recall of iCross™ Coronary Imaging Catheters

Report on Device Recalls Criticizes Current FDA Approval Process

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