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News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

News Daily News

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

Caitlin E. Cox

April 13, 2023

News Daily News

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

Michael O'Riordan

October 17, 2022

News Daily News

For Angina Patients, Language Barriers Can Complicate CVD Care

Caitlin E. Cox

December 20, 2021

News Daily News

Penumbra’s JET 7 Recall: A Kick Start to Change?

Caitlin E. Cox

December 01, 2021

News Daily News

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Michael O'Riordan

September 23, 2021

News Features

Virtual Training Booms as COVID-19 Limits In-Person Proctoring, Observation

Yael L. Maxwell

April 21, 2021

News Daily News

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

News Daily News

Hydroxychloroquine Fails to Prevent COVID-19 in Those Exposed to the Virus: RCT

Caitlin E. Cox

June 05, 2020

News Daily News

Gender Gaps Persist in CV Research, Editorships, and Training

Yael L. Maxwell

February 20, 2020

News Features

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

Marcus A. Banks

August 15, 2019

News Daily News

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell

June 18, 2019

News Conference News SCAI 2019

TAVR Operators: Can One Do It All or Are Two Still Justified?

Yael L. Maxwell

June 04, 2019

News Daily News

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

Todd Neale

November 26, 2018

News Daily News

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

L.A. McKeown

April 20, 2018

News Features

#CardiologyToo? Sexual Harassment Also Infects Hospital Corridors and the Cath Lab

Yael L. Maxwell

January 19, 2018

News Features

A Heart to Hold: 3-D Printers Add New Dimension to the Treatment of Structural Cardiac Disease

Yael L. Maxwell

August 02, 2017

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Little Pre- and Postmarket Testing for Most Recalled CV Devices

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

For Angina Patients, Language Barriers Can Complicate CVD Care

Penumbra’s JET 7 Recall: A Kick Start to Change?

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Virtual Training Booms as COVID-19 Limits In-Person Proctoring, Observation

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Hydroxychloroquine Fails to Prevent COVID-19 in Those Exposed to the Virus: RCT

Gender Gaps Persist in CV Research, Editorships, and Training

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

TAVR Operators: Can One Do It All or Are Two Still Justified?

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

#CardiologyToo? Sexual Harassment Also Infects Hospital Corridors and the Cath Lab

A Heart to Hold: 3-D Printers Add New Dimension to the Treatment of Structural Cardiac Disease

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