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News Breaks
July 2, 2014
08:13 EDTSTJSt. Jude Medical resolves FDA warning letter for Sylmar facility
St. Jude Medical announced that it has been notified by the U.S. Food and Drug Administration that issues cited in the Sylmar, California facility’s warning letter have been addressed. The company said, “We take our responsibility as a medical device manufacturer very seriously. We are encouraged by the resolution of the FDA’s warning letter and will continue to work to ensure the highest standards are met across our manufacturing facilities. St. Jude Medical is committed to providing our patients, customers and regulators with products and services that meet or exceed their expectations of safety, high-quality performance, reliability and service.”
News For STJ From The Last 14 Days
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July 29, 2014
10:00 EDTSTJOn The Fly: Analyst Initiation Summary
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06:43 EDTSTJSt. Jude Medical initiated with a Neutral at Sterne Agee
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July 28, 2014
11:07 EDTSTJLeerink medical devices analyst holds an analyst/industry conference call
Medical Devices Analyst Antalffy, along with MEDACorp Specialist Arie Pieter Kappetein, MD, PhD and Bernhard Meier, MD, assess EU cardiology trends on an Analyst/Industry conference call to be held on July 31 at 3 pm.
July 23, 2014
07:45 EDTSTJSt. Jude Medical management to meet with Deutsche Bank
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July 22, 2014
08:02 EDTSTJSt. Jude announces FlexAbility Ablation Catheter CE Mark approval, first use
St. Jude Medical CE Mark approval and first use of the FlexAbility Ablation Catheter. Designed with feedback from physician thought-leaders around the world, the FlexAbility catheter combines a unique, irrigated flexible catheter tip with a state-of-the-art handle and catheter design. The next-generation flexible tip technology was designed to reduce complications associated with ablation procedures through its ability to bend and conform to the cardiac anatomy, decreasing the amount of pressure distributed to a patient’s heart wall while simultaneously increasing the stability of therapy delivery.

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