News | Cardiovascular Business
A new report from the U.S. Food and Drug Administration (FDA) discusses the continued quality, safety and effectiveness of servicing of medical devices by original equipment manufacturers (OEMs) and third-party entities.
June 07, 2018
News | Stroke
June 7, 2018 — Results from an international clinical trial show that combining clopidogrel and aspirin following a ...
June 07, 2018
News | Embolic Protection Devices
June 7, 2018 — The first clinical cases have been completed where the Emboliner Embolic Protection Catheter was used ...
June 07, 2018Sponsored Content
Feature | Information Technology
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
March 21, 2024
Sponsored Content | Case Study | Radiation Dose Management
Radiation dose management is central to child patient safety. Medical imaging plays an increasing role in the accurate ...
June 07, 2018
June 6, 2018 — Maquet Datascope Corp. said it is recalling the CardioSave Hybrid Intra-aortic Balloon Pump (IABP) due to ...
June 06, 2018
Feature | Angiography | Dave Fornell, Editor
June 6, 2018 — Here is a checklist of dose-sparing practices for angiographic X-ray imaging used in the cath lab. This ...
June 06, 2018Sponsored Content
Feature | Cardiac Imaging
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
March 05, 2024
Technology | PET-CT
June 5, 2018 — The U.S. Food and Drug Administration (FDA) has cleared the Biograph Vision, a new positron emission ...
June 05, 2018
News | EP Lab
June 5, 2018 — Philips Healthcare has signed an agreement to acquire EPD Solutions, a provider of image-guidance in ...
June 05, 2018
Feature | Information Technology
June 5, 2018 — The future of cardiovascular care will be transformed by advances in artificial intelligence, digital ...
June 05, 2018Sponsored Content
Blog
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
December 11, 2023
Feature | Ventricular Assist Devices (VAD)
June 4, 2018 — The U.S. Food and Drug Administration said Medtronic initiated a Class 1 recall all 204,017 of its ...
June 04, 2018
Feature | Radiation Dose Management | Dave Fornell, Editor
A new consensus document on how to mitigate radiation exposure in cardiac imaging for both patients and staff was issued ...
June 01, 2018
News | Heart Valve Technology
June 1, 2018 – Use of the Abbott Portico transcatheter aortic valve replacement (TAVR) therapy was associated with ...
June 01, 2018Sponsored Content
Case Study | Hemodynamic Monitoring Systems
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
November 14, 2023
The U.S. Food and Drug Administration (FDA) is issuing a proposed order to reclassify certain radiological medical image analyzers, or computer-aided detection (CAD) devices, from class III to class II devices. This includes CAD devices for mammography breast cancer, ultrasound breast lesions and radiograph lung nodules.
June 01, 2018
Feature | Dave Fornell, Editor
June 1, 2018 — Here is the list of the most popular content on the Diagnostic and Interventional Cardiology (DAIC) ...
June 01, 2018
News | Stents Drug Eluting
Late-breaking trial results presented at the EuroPCR Congress, May 21-24 in Paris, France, found the Optimax titanium-nitride-oxide (TiNO)-coated Optimax stent was superior to the Synergy everolimus-eluting stent (EES) in acute coronary syndrome (ACS) patients. Results were presented by Pasi Karjalainen, M.D., Heart Center, Satakunta Central Hospital, Pori, Finland.
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