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Medtronic Announces CE Mark for Recapturable CoreValve Evolut R System

September 03, 2014

News Industry News

Two Year Data from FAME 2 Trial Shows Sustained Benefits of FFR-Guided PCI over Medical Treatment in Patients with Stable CAD

September 02, 2014

News Industry News

New Clinical Trial Results Demonstrate Importance of St. Jude Medical Fractional Flow Reserve in Guiding Treatment of NSTEMI Patients

September 01, 2014

News Industry News

Large-scale Study Confirms Growing Body of Clinical Evidence for the St. Jude Medical Quadripolar System

August 31, 2014

News Industry News

Boston Scientific Announces Primary Endpoint Results of NECTAR-HF Clinical Trial

August 30, 2014

News Industry News

Medtronic Announces First Implants in Largest-Ever, Global Trial of Cardiac Resynchronization Therapy

August 27, 2014

News Industry News

The ARROW® VPS G4™ Device, a Vascular Positioning System from Teleflex, Streamlines Placement of Central IV Catheters, Study Reports

August 25, 2014

News Industry News

Medtronic Viva® Cardiac Resynchronization Therapy-Pacemaker Now Available in U.S.

August 25, 2014

News Industry News

CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

August 19, 2014

News Industry News

The Lancet: Remote Monitoring Can Save ICD and CRT-D Patients’ Lives

August 15, 2014

News Industry News

Access to Abbott's MitraClip® System Expands in the U.S. with Medicare National Coverage Determination

August 12, 2014

News Industry News

Published robotic PCI study reveals favorable results with respect to patient radiation exposure, fluoroscopy time, and contrast volume

August 07, 2014

News Industry News

Medtronic Receives FDA Approval for Attain Performa® Quadripolar Lead and Viva® Quad CRT-Ds in United States

August 07, 2014

News Industry News

CardioMEMS Heart Failure Monitoring System Receives Approval from CMS for New Technology Add-On Payment

August 05, 2014

News Industry News

Teleflex Receives FDA Clearance for 150 cm Length Arrow® GPSCath® Balloon Dilatation Catheters

July 29, 2014

News Industry News

Sorin Group Announces CE Mark Approval for CROWN PRT(TM) Heart Valve

July 24, 2014

News Industry News

Radiation Exposure Concerns, Increased Precision Driving Growth of Corindus Vascular Robotics

July 23, 2014

News Industry News

St. Jude Medical Announces CE Mark Approval and First Use of the FlexAbility Ablation Catheter

July 22, 2014

News Industry News

Results of first-in-human study of Transcatheter Technologies’ TAVI device, TRINITY, are reported in(1)

July 22, 2014

News Industry News

Results of first-in-human study of Transcatheter Technologies’ TAVI device, TRINITY, are reported in EuroIntervention

July 22, 2014

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Medtronic Announces CE Mark for Recapturable CoreValve Evolut R System

Two Year Data from FAME 2 Trial Shows Sustained Benefits of FFR-Guided PCI over Medical Treatment in Patients with Stable CAD

New Clinical Trial Results Demonstrate Importance of St. Jude Medical Fractional Flow Reserve in Guiding Treatment of NSTEMI Patients

Large-scale Study Confirms Growing Body of Clinical Evidence for the St. Jude Medical Quadripolar System

Boston Scientific Announces Primary Endpoint Results of NECTAR-HF Clinical Trial

Medtronic Announces First Implants in Largest-Ever, Global Trial of Cardiac Resynchronization Therapy

The ARROW® VPS G4™ Device, a Vascular Positioning System from Teleflex, Streamlines Placement of Central IV Catheters, Study Reports

Medtronic Viva® Cardiac Resynchronization Therapy-Pacemaker Now Available in U.S.

CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

The Lancet: Remote Monitoring Can Save ICD and CRT-D Patients’ Lives

Access to Abbott's MitraClip® System Expands in the U.S. with Medicare National Coverage Determination

Published robotic PCI study reveals favorable results with respect to patient radiation exposure, fluoroscopy time, and contrast volume

Medtronic Receives FDA Approval for Attain Performa® Quadripolar Lead and Viva® Quad CRT-Ds in United States

CardioMEMS Heart Failure Monitoring System Receives Approval from CMS for New Technology Add-On Payment

Teleflex Receives FDA Clearance for 150 cm Length Arrow® GPSCath® Balloon Dilatation Catheters

Sorin Group Announces CE Mark Approval for CROWN PRT(TM) Heart Valve

Radiation Exposure Concerns, Increased Precision Driving Growth of Corindus Vascular Robotics

St. Jude Medical Announces CE Mark Approval and First Use of the FlexAbility Ablation Catheter

Results of first-in-human study of Transcatheter Technologies’ TAVI device, TRINITY, are reported in(1)

Results of first-in-human study of Transcatheter Technologies’ TAVI device, TRINITY, are reported in EuroIntervention

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