By Matt Grossman

 

Abbott Laboratories has received approval from the Food and Drug Administration for implantable devices for patients with heart-rhythm disorders, the company said Monday.

The approval covers the company's cardioverter defibrillator and resynchronization-therapy defibrillator devices. The devices include Bluetooth technology and a smartphone app to improve monitoring capability.

The devices are used to reduce the risks of arrythmias and restore the heart's natural beating pattern if the heart's chambers beat out of sync, Abbott said.

 

Write to Matt Grossman at matt.grossman@wsj.com

 

(END) Dow Jones Newswires

July 06, 2020 07:55 ET (11:55 GMT)

Copyright (c) 2020 Dow Jones & Company, Inc.
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