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FDA clears Surefire Medical Angiographic catheter line

The US Food and Drug Administration (FDA) has granted 510(k) clearance to Surefire Medical's new line of Angiographic catheters.

Angiographic Catheter line features a large inner lumen of 0.054 inches which enables interventional radiologists to gain access to various patient anatomies by using different curve styles.

Surefire Medical CEO Jim Chomas said the company has designed a line of Angiographic catheters to help advance interventional radiology procedures by providing optimal diagnostic imaging and detail during infusion procedures.

"We are excited to offer a suite of products to better meet their clinical needs," Chomas added.

"Further, the large inner lumen provides a new level of flexibility to these physicians."

In addition, the company has received FDA’s 510(k) clearance for its Surefire Infusion system and new Surefire ST and LT infusion systems, which increase the efficiency of targeted treatments.