FierceBiotech4d
J&J MedTech secures FDA approval for Varipulse pulsed field ablation system
Johnson & Johnson MedTech will enter the U.S. pulsed field ablation market following an FDA green light for its Varipulse ...
emjreviews.com4d
FDA nod for Johnson & Johnson’s atrial fibrillation device
Johnson & Johnson MedTech has received FDA approval for its device for drug-refractory paroxysmal atrial fibrillation.
Medtronic Gets FDA Approval for Affera Technology
Medtronic said the Food and Drug Administration approved its Affera mapping and ablation system with sphere-9 catheter.
Yahoo3d
The Apple Watch is helping Afib patients ditch blood thinners in a ground-breaking trial
A hospital in Pittsburgh has become the latest medical center to join a ground-breaking Apple Watch trial in the US that's ...
medtechdive4d
J&J wins FDA approval for Varipulse PFA system
J&J is the third medtech company to gain U.S. approval for pulsed field ablation, a new atrial fibrillation treatment seeing rapid adoption.
FierceBiotech21d
Boston Scientific’s navigation-equipped pulsed field ablation catheter passes FDA
Boston Scientific collected a set of FDA green lights for an update to its pulsed field ablation system for atrial fibrillation, allowing it to combine cardiac mapping sensors and therapy delivery ...
Nasdaq18d
A new paradigm in electrophysiology: Medtronic receives FDA approval of Affera™ Mapping and Ablation System and Sphere-9™ Catheter
Medtronic is now the first and only company with two PFA technologies available for patients with Afib. The PulseSelect™ Pulsed Field Ablation System, which was FDA approved in December 2023 ...
KHON227d
XYRA Announces FDA Label Guidance for Managing Atrial Fibrillation with Budiodarone and Wearable Monitoring Devices
The FDA has agreed on the use of AF monitoring devices in clinical trials for budiodarone approval ... and maintaining normal sinus rhythm. Atrial Fibrillation (AF) is the most common sustained ...