Thursday, May 20, 2010

US FDA warns St. Jude on Heart Device Claims

Device maker St Jude Medical Inc made improper claims about two heart devices, U.S. regulators said in a letter to the company.

The Food and Drug Administration, in an April 23 letter, objected to statements made on a company website about the Epicor LP Cardiac Ablation System and the Epicor UltraCinch LP Ablation Device.

More here.