DUBLIN, July 21, 2016 /PRNewswire/ —Vasorum Ltd. The developer and manufacturer of the novel Celt ACD vascular closure device has received approval of its PMA application from the US Food and Drug Administration (FDA). Celt ACD, which previously received CE mark and is sold in Europe, is indicated for arterial puncture closure in both diagnostic and anticoagulated percutaneous interventional cardiology and radiology patients. Celt ACD offers excellent time to hemostasis in a wide variety of clinical situations. A randomized controlled clinical trial which recruited 207 interventional cardiology procedure patients was carried out in four International Cardiology Centres across US and Europe. The trial’s Principal Investigator was Dr. Shing-Chiu Wong, Director of Cardiac…
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