2005

Study Designed to Evaluate the Safety and Efficacy of Surgical Microwave Ablation Technology to Treat Common Heart Arrhythmia Indianapolis, Ind. and Santa Clara, Calif. - Guidant Corporation...

Guidant Reiterates its Previous Physician and Patient Recommendations Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) said today that FDA has classified its June 17, 2005 and June 24, 2005...

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) said today it is voluntarily advising physicians about important safety information regarding certain devices. Guidant apprised FDA of this...

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) today announced its intention to establish an independent panel of experts to recommend guidelines for when to disseminate information to...

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) said today it is voluntarily advising physicians about important safety information regarding certain devices. Guidant has apprised FDA of...

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) initiated a communication to physicians regarding the clinical performance of its VENTAK PRIZM® 2 DR Model 1861 implantable defibrillator....

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) today announced that it has received Investigational Device Exemption (IDE) conditional approval from the U.S. Food and Drug Administration...

Indianapolis, Ind. - Guidant Corporation (NYSE: GDT) announced that at a special meeting of shareholders held today in Indianapolis, Guidant shareholders overwhelmingly approved the agreement...

New Brunswick, N.J., and Indianapolis, Ind. - Johnson & Johnson and Guidant Corporation today announced that they have been notified, as anticipated, that the European Commission has decided to...

Company Completes Several Merger-Related Milestones During Quarter Sales of products other than worldwide coronary stents were $838 million, up 10 percent Worldwide implantable defibrillator...

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