Defibrillators (ICDs) for Heart Arrhythmias | Abbott
Abbott Receives FDA Approval for World's First Dual Chamber Leadless Pacemaker
FDA Warns on Abbott's St. Jude Pacemakers and Defibrillators - WSJ
FDA Recalls Abbott Implantable Defibrillators for Faulty Wires
St. Jude Medical Played Down Defibrillator Failures for Years, F.D.A. Says - The New York Times
Device maker ignored defibrillator defect that killed patients, FDA says | Healthcare Finance News
About the app - My Heart Health
Abbott Recalls Ellipse Implantable Cardioverter Defibrillators Due to Exposed Aluminum Wires | DAIC
Study finds fault with ICD leads that Abbott inherited from St. Jude Medical - Medical Design and Outsourcing
I Do Feel Really Lucky Just to be Alive." | Abbott Newsroom
FDA Clears Abbott Gallant ICD and CRT With Bluetooth Connectivity and Continuous Remote Monitoring | DAIC
Implantable Cardioverter Defibrillators | Abbott
Abbott Levels-Up Wireless Pacemaker Tech | Abbott Newsroom
ICD and CRT-D Solutions | Abbott
Implantable Cardioverter Defibrillators | Abbott
Abbott Announces MR-Conditional Labeling for Quadra Assura CRT-D and Fortify Assura ICD | DAIC
Abbott Issues New Updates for Implanted Cardiac Devices | Sudden Cardiac Arrest Foundation
FDA clears Abbott's Gallant devices for cardiac arrhythmia
Ellipse (defibrillator)
Implantable Cardioverter Defibrillators | Abbott
Taking Care of Your Heart | Abbott Newsroom
St. Jude Medical Defibrillators - Devices at Risk, Recalls
New £1.8m clinical trial to help reduce sudden cardiac deaths using implantable defibrillators | Southampton Clinical Trials Unit | University of Southampton
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