Covidien receives FDA clearance for Mallinckrodt TaperGuard Evac endotracheal tube
Covidien has received clearance from the FDA to market a medical device, called the Mallinckrodt TaperGuard Evac endotracheal tube, created to reduce the risk of postsurgical complications caused by the aspiration of fluids into the lungs. Although complications from pulmonary aspiration are rare, the consequences can be severe, Covidien said.
-
Covidien receives FDA nod for surgery kit for laparoscopic procedures
FDA clears Covidien Leak Compensation software
SafeStitch Medical, Inc. Receives FDA Clearance to Market the AMID StaplerTM for Hernia Repairs
ArthroCare Receives FDA Clearance for Parallax Contour Vertebral Augmentation Device
Covidien releases Evidentâ„¢ microwave ablation system
