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Medtronic Announces Approval and Launch of Reveal LINQ(TM) Insertable Cardiac Monitor in Japan

September 14, 2016

News Industry News

EDWARDS INTUITY Elite Rapid Deployment Valve Receives FDA Approval

August 15, 2016

News Industry News

Resverlogix Announces Positive Recommendation From Data Safety Monitoring Board For Phase 3 Study of Apabetalone (RVX-208)

August 11, 2016

News Industry News

Edwards Receives Approval For SAPIEN 3 Heart Valve In Canada

July 28, 2016

News Industry News

BIOTRONIK Launches CardioMessenger Smart Portable Device For Pacemaker and ICD Patients

May 24, 2016

News Industry News

BIOTRONIK Announces FDA Approval of MR Conditional Cardiac Resynchronization Defibrillators

May 04, 2016

News Industry News

Medtronic Receives FDA Approval for New Single-Chamber ICDs That Detect Atrial Fibrillation

May 02, 2016

News Industry News

HeartWare Completes Enrollment In HVAD® System LATERAL Study™

April 28, 2016

News Industry News

Boston Scientific Receives U.S. FDA Approval For ImageReady™ MR-Conditional Pacing System

April 26, 2016

News Industry News

Real-World Study Shows 72 Percent of Atrial Fibrillation Would Have Gone Undiagnosed in Stroke Patients if Cardiac Monitoring Had Been Limited to 30 Days

April 20, 2016

News Industry News

Stroke Prevention: BIOTRONIK Announces FDA Approval of BioMonitor 2 Insertable Cardiac Monitor

April 12, 2016

News Industry News

FDA Approves World's Smallest Pacemaker for U.S. Patients

April 07, 2016

News Industry News

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

March 06, 2016

News Industry News

APN Health Receives FDA Clearance for Innovative Cardiac Mapping System

February 25, 2016

News Industry News

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

January 14, 2016

News Industry News

FDA Approves BIOTRONIK Iperia ICD Systems with Full-Body ProMRI Technology

December 21, 2015

News Industry News

Medtronic Announces FDA Approval and Launch of World's First App-Based Remote Monitoring System for Pacemakers

November 16, 2015

News Industry News

Medtronic Receives CE Mark for New Single-Chamber ICDs That Can Detect Atrial Fibrillation

October 21, 2015

News Industry News

Early Human Cases With Edwards FORMA Tricuspid Repair System Presented At TCT

October 14, 2015

News Industry News

Medtronic First to Receive FDA Approval for MR-Conditional Implantable Cardioverter Defibrillator System

September 15, 2015

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Medtronic Announces Approval and Launch of Reveal LINQ(TM) Insertable Cardiac Monitor in Japan

EDWARDS INTUITY Elite Rapid Deployment Valve Receives FDA Approval

Resverlogix Announces Positive Recommendation From Data Safety Monitoring Board For Phase 3 Study of Apabetalone (RVX-208)

Edwards Receives Approval For SAPIEN 3 Heart Valve In Canada

BIOTRONIK Launches CardioMessenger Smart Portable Device For Pacemaker and ICD Patients

BIOTRONIK Announces FDA Approval of MR Conditional Cardiac Resynchronization Defibrillators

Medtronic Receives FDA Approval for New Single-Chamber ICDs That Detect Atrial Fibrillation

HeartWare Completes Enrollment In HVAD® System LATERAL Study™

Boston Scientific Receives U.S. FDA Approval For ImageReady™ MR-Conditional Pacing System

Real-World Study Shows 72 Percent of Atrial Fibrillation Would Have Gone Undiagnosed in Stroke Patients if Cardiac Monitoring Had Been Limited to 30 Days

Stroke Prevention: BIOTRONIK Announces FDA Approval of BioMonitor 2 Insertable Cardiac Monitor

FDA Approves World's Smallest Pacemaker for U.S. Patients

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

APN Health Receives FDA Clearance for Innovative Cardiac Mapping System

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

FDA Approves BIOTRONIK Iperia ICD Systems with Full-Body ProMRI Technology

Medtronic Announces FDA Approval and Launch of World's First App-Based Remote Monitoring System for Pacemakers

Medtronic Receives CE Mark for New Single-Chamber ICDs That Can Detect Atrial Fibrillation

Early Human Cases With Edwards FORMA Tricuspid Repair System Presented At TCT

Medtronic First to Receive FDA Approval for MR-Conditional Implantable Cardioverter Defibrillator System

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