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October 12, 2016

FDA Clears Teleflex's Arrow JACC With Chloragard Technology and Tunneler

October 12, 2016—Teleflex Incorporated announced that it has received US Food and Drug Administration 510(k) clearance to market the company’s Arrow JACC (jugular axillosubclavian central catheter) with Chloragard technology and TightTrack tunneler.

According to Teleflex, the Arrow JACC with Chloragard is a long-term, tunneled, small French-size antithrombogenic and antimicrobial central venous catheter designed to meet the needs of patients throughout their course of therapy or illness. The catheter is also designed for use with high-pressure injection for diagnostic studies.

Arrow JACC with Chloragard protects against catheter occlusion, phlebitis, and intimal hyperplasia for up to 30 days. It also enables caregivers to effectively and economically preserve vessel access and care for end-stage renal disease patients, stated the company.

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October 12, 2016

Sirtex Microspheres to Be Studied for Cholangiocarcinoma in SIRCCA and Included in ESMO Guidelines

October 11, 2016

Prof. Ian Meredith to Join Boston Scientific as Global Chief Medical Officer