Surefire Medical, Inc, announced that the company has received 510(k) FDA clearance to market its line of Surefire Angiographic Catheters. Surefire Medical will launch these products in the United States later this year.
Surefire’s Angiographic Catheter line is designed to provide interventional radiologists with greater flexibility and the highest level of trackability when performing infusion procedures. The catheters have a large inner lumen of 0.054 inches and will be available in a variety of different curve styles for accessing a wide range of patient anatomies.
This is the third FDA 510(k) clearance received by Surefire Medical since July 2011. ■