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Spectranetics Announces FDA Submission of Bridge(TM) Occlusion Balloon for Lead Extraction Procedures

December 08, 2015

News Daily News

Sugary Drinks an Increasing Threat to Global Cardiometabolic Health

Todd Neale

December 02, 2015

News Industry News

Amsel Medical Corporation Announces Filing of 2nd 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device

October 27, 2015

News Industry News

Regeneron and Sanofi Announce CHMP Recommends European Approval of Praluent® (alirocumab) for the Treatment of Hypercholesterolemia

July 24, 2015

News Industry News

NICE recommends once-daily LIXIANA® (edoxaban) for the treatment and prevention of recurrent Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) in adults

July 13, 2015

News Industry News

Regeneron and Sanofi Announce Phase 3 Results Showing LDL-C Reductions of More Than 60 Percent in Japanese Patients Treated with Praluent® (alirocumab) Injection

July 09, 2015

News Industry News

Boehringer Ingelheim Initiates U.S. Sites in First-Ever Global Phase III Trial of Investigational Antidote in Patients Taking PRADAXA®

November 09, 2014

News Industry News

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

July 10, 2014

News Industry News

FDA Approves BIOTRONIK Entovis Pacemaker System with ProMRI® Technology

May 07, 2014

News Industry News

Medtronic to Appeal Federal District Court Ruling

April 11, 2014

News Industry News

MediValve, Ltd., Announces Clearance of a 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the acWire™ Guidewire

January 12, 2014

News Daily News

Nonvalvular A-fib Patients More Likely to Remain on Dabigatran Than Warfarin

Jason Kahn

August 12, 2013

News Industry News

BIOTRONIK continues 50-year legacy of engineering excellence with smaller, thinner ICD/CRT-D, including the unique DX platform

May 08, 2013

News Daily News

Italian Generic Clopidogrel Worse Than Brand Name at Suppressing Platelets

Jason Kahn

December 13, 2012

News Industry News

Cook Medical’s Zilver® PTX® Earns FDA Approval As First Drug-Eluting Stent in U.S. to Treat Peripheral Arterial Disease

November 14, 2012

News Industry News

STENTYS Receives FDA Approval to Initiate First U.S. Clinical Trial With Self-Apposing® Stent

October 22, 2012

News Industry News

Boston Scientific Launches Emerge™ PTCA Balloon Dilatation Catheter in the U.S.

September 27, 2012

News Daily News

Clot Retrieval Devices Show Improved Results in Acute Ischemic Stroke Patients

Jason Kahn

August 31, 2012

News Daily News

TAVR Use Outstrips Evidence in Europe, BMJ Analysis Says

August 02, 2012

News Industry News

Study of First-in-Class WATCHMAN® Device Shows 75 Percent Reduction in Stroke Risk in Patients with Atrial Fibrillation Not Eligible for Oral Anticoagulation Therapy

May 11, 2012

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Spectranetics Announces FDA Submission of Bridge(TM) Occlusion Balloon for Lead Extraction Procedures

Sugary Drinks an Increasing Threat to Global Cardiometabolic Health

Amsel Medical Corporation Announces Filing of 2nd 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device

Regeneron and Sanofi Announce CHMP Recommends European Approval of Praluent® (alirocumab) for the Treatment of Hypercholesterolemia

NICE recommends once-daily LIXIANA® (edoxaban) for the treatment and prevention of recurrent Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) in adults

Regeneron and Sanofi Announce Phase 3 Results Showing LDL-C Reductions of More Than 60 Percent in Japanese Patients Treated with Praluent® (alirocumab) Injection

Boehringer Ingelheim Initiates U.S. Sites in First-Ever Global Phase III Trial of Investigational Antidote in Patients Taking PRADAXA®

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

FDA Approves BIOTRONIK Entovis Pacemaker System with ProMRI® Technology

Medtronic to Appeal Federal District Court Ruling

MediValve, Ltd., Announces Clearance of a 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the acWire™ Guidewire

Nonvalvular A-fib Patients More Likely to Remain on Dabigatran Than Warfarin

BIOTRONIK continues 50-year legacy of engineering excellence with smaller, thinner ICD/CRT-D, including the unique DX platform

Italian Generic Clopidogrel Worse Than Brand Name at Suppressing Platelets

Cook Medical’s Zilver® PTX® Earns FDA Approval As First Drug-Eluting Stent in U.S. to Treat Peripheral Arterial Disease

STENTYS Receives FDA Approval to Initiate First U.S. Clinical Trial With Self-Apposing® Stent

Boston Scientific Launches Emerge™ PTCA Balloon Dilatation Catheter in the U.S.

Clot Retrieval Devices Show Improved Results in Acute Ischemic Stroke Patients

TAVR Use Outstrips Evidence in Europe, BMJ Analysis Says

Study of First-in-Class WATCHMAN® Device Shows 75 Percent Reduction in Stroke Risk in Patients with Atrial Fibrillation Not Eligible for Oral Anticoagulation Therapy

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