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Vascular Solutions Recalls Twin-Pass Dual-Access Catheters

Michael O'Riordan

October 06, 2016

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for August 2016

September 01, 2016

News Daily News

‘Shotgunning’ Approach Appears to Knock Down Readmissions After PCI

August 25, 2016

News Daily News

FDA: Angiographic Catheter Recalled Due to Potential Tip Separation

July 22, 2016

News Daily News

Now You See It: FDA Approves Absorb Bioresorbable Scaffold

Michael O'Riordan

July 05, 2016

News Daily News

Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls

July 05, 2016

News Industry News

BIOTRONIK Launches CardioMessenger Smart Portable Device For Pacemaker and ICD Patients

May 24, 2016

News Daily News

Cook Medical Issues Recall for Beacon Tip Catheters

May 04, 2016

News Daily News

Un Comité Asesor de la FDA Rechaza el Monitor Intercardíaco AngelMed Guardian

March 17, 2016

News Daily News

FDA 顾问委员会拒绝批准 AngelMed Guardian 心腔内监护仪

March 17, 2016

News Daily News

FDA Advisory Committee Rejects AngelMed Guardian Intracardiac Monitor

March 17, 2016

News Industry News

Medtronic Receives CE Mark for New Single-Chamber ICDs That Can Detect Atrial Fibrillation

October 21, 2015

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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