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Cook Medical reintroduces its Evolution® RL lead extraction products to the United States market

July 10, 2014

News Industry News

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

July 03, 2014

News Industry News

Bristol-Myers Squibb Issues Voluntary Nationwide Recall of COUMADIN® (warfarin sodium) FOR INJECTION Due to Presence of Particulate Matter

June 30, 2014

News Daily News

Un Estudio Pone de Manifiesto la Disparidad entre Resultados de Estudios Pre y Post-Comercialización sobre SLF

Caitlin E. Cox

June 13, 2014

News Daily News

Study Highlights Disparity Between Pre-, Postmarket Study Outcomes for DES

Caitlin E. Cox

June 13, 2014

News Industry News

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

May 12, 2014

News Daily News

Leaders from NIH, FDA, Academia Urge US Government to Invest in Medical Innovation

L.A. McKeown

May 09, 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

Los Dispositivos Cardiovasculares son la Clase Más Amplia de Dispositivo Retirados por la FDA desde 2005

Yael L. Maxwell

April 03, 2014

News Daily News

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

L.A. McKeown

October 14, 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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Cook Medical reintroduces its Evolution® RL lead extraction products to the United States market

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

Bristol-Myers Squibb Issues Voluntary Nationwide Recall of COUMADIN® (warfarin sodium) FOR INJECTION Due to Presence of Particulate Matter

Un Estudio Pone de Manifiesto la Disparidad entre Resultados de Estudios Pre y Post-Comercialización sobre SLF

Study Highlights Disparity Between Pre-, Postmarket Study Outcomes for DES

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

Leaders from NIH, FDA, Academia Urge US Government to Invest in Medical Innovation

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

Los Dispositivos Cardiovasculares son la Clase Más Amplia de Dispositivo Retirados por la FDA desde 2005

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

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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