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‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

L.A. McKeown

September 18, 2023

News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood

July 26, 2023

News Daily News

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Shelley Wood

December 16, 2020

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

Todd Neale

April 25, 2019

News Daily News

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

L.A. McKeown

November 29, 2018

News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Todd Neale

July 21, 2017

News Daily News

FDA’s Latest Move Against Aspirin for CVD Primary Prevention: A Picture Is Worth 11 Words

Shelley Wood

January 13, 2017

News Daily News

FDA Expands Indications for Two Endovascular Stroke Therapies

Todd Neale

September 06, 2016

News Daily News

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

Yael L. Maxwell

September 02, 2016

News Daily News

FDA Declines to Approve Portola’s Reversal Agent for Factor Xa Inhibitors

Michael O'Riordan

August 18, 2016

News Daily News

La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA

Yael L. Maxwell

July 17, 2015

News Daily News

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

Yael L. Maxwell

July 17, 2015

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

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‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

TCTMD’s Top 10 Most Popular Stories for April 2019

FDA Warns Against Off-label Use of Wingspan Stent System

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

FDA’s Latest Move Against Aspirin for CVD Primary Prevention: A Picture Is Worth 11 Words

FDA Expands Indications for Two Endovascular Stroke Therapies

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

FDA Declines to Approve Portola’s Reversal Agent for Factor Xa Inhibitors

La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

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