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FDA Approves Cordella Remote PA Pressure Monitoring System for HF

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FDA Approves Cordella Remote PA Pressure Monitoring System for HF

Yael L. Maxwell

June 24, 2024

FDA Approves Bioresorbable Scaffold for BTK Lesions

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FDA Approves Bioresorbable Scaffold for BTK Lesions

Michael O'Riordan

April 29, 2024

FDA Approves TriClip TEER Device for Tricuspid Repair

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FDA Approves TriClip TEER Device for Tricuspid Repair

April 02, 2024

FDA Approves First Transcatheter Tricuspid Valve Replacement Device

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FDA Approves First Transcatheter Tricuspid Valve Replacement Device

February 02, 2024

FDA Approves Next-Generation Watchman FLX Device for LAA Occlusion

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FDA Approves Next-Generation Watchman FLX Device for LAA Occlusion

July 22, 2020

Details in Print for DanGer Design as Impella AMICS RCT Expands From Denmark to Germany

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Details in Print for DanGer Design as Impella AMICS RCT Expands From Denmark to Germany

May 14, 2019

FDA Extends MitraClip Indication to Include Functional MR

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FDA Extends MitraClip Indication to Include Functional MR

March 14, 2019

FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies

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FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies

January 14, 2019

FDA Advisors Give Blessing to Implantable Pulse Generator in Certain Heart Failure Patients

News Daily News

FDA Advisors Give Blessing to Implantable Pulse Generator in Certain Heart Failure Patients

Yael L. Maxwell

December 05, 2018

FDA Puts the Kibosh on Canakinumab for Cardiac Indication—at Least for Now

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FDA Puts the Kibosh on Canakinumab for Cardiac Indication—at Least for Now

Michael O'Riordan

November 01, 2018

News Daily News

TAVR as an Option for Intermediate-Risk Patients: Physicians Respond

Yael L. Maxwell

August 24, 2016

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