FREMONT, Calif.--(BUSINESS WIRE)-- Cordis Corporation today announced it has received clearance from the Food and Drug Administration of its latest innovation in guiding catheters: the ADROIT TM 6F ...
The FDA determined this week that Cordis’ recent recall of several versions of its Super Torque angiographic catheters meet the criteria of a Class I recall, a label reserved for those the agency ...
FREMONT, Calif.--(BUSINESS WIRE)--Cordis Corporation announced today that it has entered into an agreement with TriReme Medical, Inc. that grants the company exclusive distribution rights for the ...
Cordis Corp., Johnson & Johnson's stenting arm, notched another 510(k) clearance for its Adroit 6F Guiding Catheter, which the company says can handle more sophisticated lesions. Cordis Corp., the ...
BRIDGEWATER, N.J.--(BUSINESS WIRE)-- Cordis Corporation is pleased to announce the launch of SLEEK® OTW Catheter, a new .014” Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter designed to ...
DUBLIN, Ohio - Cordis, a Cardinal Health company, recently announced the full U.S. launch of its RADIAL 360 portfolio, offering a complete range of products to facilitate the transradial approach (TRA ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results