Abbott announced U.S. Food and Drug Administration (FDA) approval for magnetic resonance (MR)-conditional labeling for one of the company's most widely-used implantable cardioverter defibrillators...
EP Lab
-
-
Fysicon announced that it has been granted 510(k) clearance by the U.S. Food and Drug Administration (FDA) for its QMAPP hemodynamic monitoring system.
-
August 29, 2017 — The U.S.
-
Biotronik announced U.S. Food and Drug Administration (FDA) approval and commercial availability of Edora HF-T QP, an MR conditional quadripolar (QP) cardiac resynchronization therapy pacemaker (...
Technology | Implantable Cardioverter Defibrillator (ICD) | September 22, 2017
September 22, 2017 — Abbott announced U.S. Food and Drug Administration (FDA) approval for...
Technology | Hemodynamic Monitoring Systems | September 18, 2017
September 18, 2017 — Fysicon announced that it has been granted 510(k) clearance by the U.S. Food and Drug...
Image courtesy of Technavio
News | EP Lab | September 11, 2017
September 11, 2017 — According to the latest market study released by Technavio, the global...
LAA closure during open heart surgery in the LAACS Study showed better outcomes for all patients.
Feature | Left Atrial Appendage (LAA) Occluders | September 07, 2017
September 7, 2017 — Closure of the left atrial appendage (LAA) during heart surgery protects the brain, according to...
News | Atrial Fibrillation | September 01, 2017
September 1, 2017 — Apixaban lowers the risk of stroke compared to warfarin in anticoagulation-naïve patients with...
The CASTLE-AF Study shows catheter alation of AF can be used effectively to treat heart failure in patients with an implanted ICD.
News | Atrial Fibrillation | September 01, 2017
September 1, 2017 — Final results from the CASTLE-AF study show a 38 percent reduction in the composite of all-cause...
Abbott. St. Jude Medical has updated its firmware to address cybersecurity issues with its Allure Quadra MP and other EP devices.
Feature | EP Lab | August 29, 2017 | Dave Fornell
August 29, 2017 — The U.S. Food and Drug Administration (FDA) approved a firmware update that is now available to...
News | Antiplatelet and Anticoagulation Therapies | August 28, 2017
August 28, 2017 — Bristol-Myers Squibb Company and Pfizer Inc. announced results from an analysis of real-world data...
Technology | Cardiac Resynchronization Therapy Devices (CRT) | August 21, 2017
August 21, 2017 — Biotronik announced U.S. Food and Drug Administration (FDA) approval and commercial availability...
Feature | Cybersecurity | August 16, 2017 | Dave Fornell
There is growing concern among patients and regulators that medical devices, especially implantable...
News | Ablation Systems | August 07, 2017
August 7, 2017 — CardioFocus Inc. announced that its HeartLight Endoscopic...
Hemodynamic data shown on screens from the Merge Hemo recording system. It is among the newer generation hemodynamic systems for cath labs that are more user friendly and have technologies to speed workflow.
Feature | Hemodynamic Monitoring Systems | August 03, 2017 | Dave Fornell
The current generation of...
News | Atrial Fibrillation | August 02, 2017
Aug. 2, 2017 — A new health economic analysis from the landmark...
News | Atrial Fibrillation | August 01, 2017
Aug. 1, 2017 — The Japanese Ministry of Health, Labour and Welfare has granted Japanese market clearance for the...
