Published in Medical Letter on the CDC and FDA, June 19th, 2005
The device is part of a state-of-the-art system that incorporates home monitoring early detection technology, biphasic II shock capability, and 36-Joule shock energy.
"The FDA approval of our Xelos DR-T high-energy ICD represents another milestone in our drive to deliver complete tachycardia solutions to our customers," said Jake Langer, president of BIOTRONIK, Inc. "The combination of our exclusive home monitoring technology and 36-Joule shock capability will further...
Want to see the full article?
Welcome to NewsRx!
Learn more about a six-week, no-risk free trial of Medical Letter on the CDC and FDA
NewsRx also is available at LexisNexis, Gale, ProQuest, Factiva, Dialog, Thomson Reuters, NewsEdge, and Dow Jones.