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Little Pre- and Postmarket Testing for Most Recalled CV Devices

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Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

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 First Extravascular ICD

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FDA Approves First Extravascular ICD

Yael L. Maxwell

October 23, 2023

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

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

Yael L. Maxwell

December 05, 2018

CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

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CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

September 05, 2018

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

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High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan

July 20, 2018

Implantable Cardiac Monitor for High-Risk ACS Patients Wins FDA Approval

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Implantable Cardiac Monitor for High-Risk ACS Patients Wins FDA Approval

Michael O'Riordan

May 08, 2018

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