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Little Pre- and Postmarket Testing for Most Recalled CV Devices

News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

Mechanism’s Mojo ‘Obvious’ CV Therapies More Likely to Be Seen as Effective

News Daily News

Mechanism’s Mojo: ‘Obvious’ CV Therapies More Likely to Be Seen as Effective

Michael O'Riordan

February 23, 2024

FDA Approves First Transcatheter Tricuspid Valve Replacement Device

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FDA Approves First Transcatheter Tricuspid Valve Replacement Device

February 02, 2024

Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

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Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

July 06, 2023

FDA Approves Portico TAVI Valve, Paving the Way for Third US Device

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FDA Approves Portico TAVI Valve, Paving the Way for Third US Device

September 20, 2021

FDA Approves Lotus Edge, Ushering Third Device Into US Market

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FDA Approves Lotus Edge, Ushering Third Device Into US Market

April 24, 2019

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

News Daily News

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

Michael O'Riordan

July 20, 2018

News Daily News

FDA Approves Next-Gen CoreValve Evolut PRO Valve

March 22, 2017

News Daily News

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

Yael L. Maxwell

August 24, 2016

News Daily News

Next-Generation CoreValve Device Receives CE Mark for Use in Intermediate-Risk Patients

August 01, 2016

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