US FDA approves Johnson & Johnson's device for heart condition

- 11/7/2024

</head><body><p>(Reuters) - The U.S. Food & Drug Administration has approved Johnson & Johnson's device for a type of condition which causes abnormal heart rhythm, the company said on Thursday.</p><p>The device, Varipulse, is a pulsed field ablation system. </p><p>Medical device makers such as Boston Scientific and Medtronic also have devices approved for atrial fibrillation, a condition that is characterized by an irregular rhythm of the heart.</p><p>The health regulator has approved the use of the J&J device for the treatment of drug refractory paroxysmal atrial fibrillation, in which the symptoms are occasional and usually last between a few minutes and hours.</p><p/><p> (This story has been corrected to remove the reference to the device's mechanism in paragraph 2)</p><p/><p> (Reporting by Sriparna Roy in Bengaluru; Editing by Shounak Dasgupta)</p></body></html></p> <div id="news-wrapper"> <div class="thumbnail additional-resources client-content-image-box"> <div class="box-image" style="background-image: url(/images/home/news.jpg);"></div> <div class="caption"> <h3>Nationwide News</h3> <div> <p><a href='/aging/news-archive.aspx'>News Archive</a></p> </div> </div> </div> </div> </div> </div> </div> </section> </div>  <footer class="footer">  <div class="clearfix footerInfo"> <div class="container"> <div class="row"> <div class="col-sm-7 col-xs-12"> <div class="footerText"> <a href="http://www.trilogyir.com/" target="_blank" class="footerLogo"><img src="/images/Noc-Logo-white.png" alt="Footer Logo" style="width: 200px;"></a> <div class="genericContent" id="landingPageText"> <p>The Network of Care is a comprehensive, Internet-based community resource for seniors and persons with disabilities, as well as their caregivers and service providers.</p> </div> <h3 id="lblTechAssistance" style="color: #fff; 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US FDA approves Johnson & Johnson's device for heart condition