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APN Health Receives FDA Clearance for Innovative Cardiac Mapping System

February 25, 2016

News Industry News

Boston Scientific Receives U.S. FDA Approval For Quadripolar Leads And Initiates Global Trial To Expand MRI Labeling To The U.S. And Asia

February 22, 2016

News Industry News

Medtronic Receives CE Mark for Full Line of Cardiac Resynchronization Therapy-Defibrillators Compatible with MRI Scans

February 21, 2016

News Daily News

Anthracycline-Based Chemotherapy Linked to Valve Disease, Even in Absence of Radiation

L.A. McKeown

February 16, 2016

News Industry News

Clear Guide Medical Wins FDA Clearance for its SCENERGY Ultrasound-CT Fusion System

February 15, 2016

News Daily News

Cardio-Oncology Offers Fellows the Opportunity to Venture Into the ‘Wild West’

L.A. McKeown

February 15, 2016

News Conference News ISET 2016

Drug-Coated Balloon Angioplasty Superior for In-Stent Restenosis of SFA, but Results Leave Much To Be Desired

Michael O'Riordan

February 10, 2016

News Industry News

St. Jude Medical Announces Launch of OPTIS Mobile System in Europe and Japan

February 07, 2016

News Industry News

Medtronic First to Receive FDA Approval for MR-Conditional Cardiac Resynchronization Therapy-Defibrillators

February 04, 2016

News Daily News

Signs of Cardioprotection Seen in Acute STEMI Patients Receiving IV Beta-blocker Post-PCI

Caitlin E. Cox

February 03, 2016

News Daily News

超声心动图使用不足（特别是急性心梗患者）与更多的医院死亡相关

Shelley Wood

February 01, 2016

News Daily News

Underuse of Echocardiography, Particularly in AMI, Linked to More In-hospital Deaths

Shelley Wood

February 01, 2016

News Daily News

Underuse of Echocardiography, Particularly in AMI, Linked to More In-hospital Deaths

Shelley Wood

February 01, 2016

News Daily News

Leaving Significant Stenoses Untreated After PCI May Worsen 1-Year Outcomes: SCAAR Data

Todd Neale

February 01, 2016

News Daily News

Study Suggests CCU Can Be Skipped for Many NSTE-ACS Patients

Todd Neale

January 28, 2016

News Industry News

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

January 14, 2016

News Industry News

Conavi Medical (formerly Colibri Technologies) announces FDA 510k clearance for its first product, the Foresight ICE System for Intracardiac Echocardiography

January 13, 2016

News Daily News

分析表明需要通过审核和反馈来遏制心脏成像的过度

Caitlin E. Cox

January 06, 2016

News Daily News

Reducir el Exceso de Imágenes Cardíacas Requiere Feedback y Controles

Caitlin E. Cox

January 06, 2016

News Daily News

Curbing Overuse of Cardiac Imaging Requires Audits and Feedback, Analysis Shows

Caitlin E. Cox

January 06, 2016

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APN Health Receives FDA Clearance for Innovative Cardiac Mapping System

Boston Scientific Receives U.S. FDA Approval For Quadripolar Leads And Initiates Global Trial To Expand MRI Labeling To The U.S. And Asia

Medtronic Receives CE Mark for Full Line of Cardiac Resynchronization Therapy-Defibrillators Compatible with MRI Scans

Anthracycline-Based Chemotherapy Linked to Valve Disease, Even in Absence of Radiation

Clear Guide Medical Wins FDA Clearance for its SCENERGY Ultrasound-CT Fusion System

Cardio-Oncology Offers Fellows the Opportunity to Venture Into the ‘Wild West’

Drug-Coated Balloon Angioplasty Superior for In-Stent Restenosis of SFA, but Results Leave Much To Be Desired

St. Jude Medical Announces Launch of OPTIS Mobile System in Europe and Japan

Medtronic First to Receive FDA Approval for MR-Conditional Cardiac Resynchronization Therapy-Defibrillators

Signs of Cardioprotection Seen in Acute STEMI Patients Receiving IV Beta-blocker Post-PCI

超声心动图使用不足（特别是急性心梗患者）与更多的医院死亡相关

Underuse of Echocardiography, Particularly in AMI, Linked to More In-hospital Deaths

Underuse of Echocardiography, Particularly in AMI, Linked to More In-hospital Deaths

Leaving Significant Stenoses Untreated After PCI May Worsen 1-Year Outcomes: SCAAR Data

Study Suggests CCU Can Be Skipped for Many NSTE-ACS Patients

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

Conavi Medical (formerly Colibri Technologies) announces FDA 510k clearance for its first product, the Foresight ICE System for Intracardiac Echocardiography

分析表明需要通过审核和反馈来遏制心脏成像的过度

Reducir el Exceso de Imágenes Cardíacas Requiere Feedback y Controles

Curbing Overuse of Cardiac Imaging Requires Audits and Feedback, Analysis Shows

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