PROGUIDE CHRONIC DIALYSIS CATHETER

PROGUIDE CHRONIC DIALYSIS CATHETER is an FDA 510(k)-cleared medical device (K090148) manufactured by Merit Medical Systems, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 12, 2009. Regulation: 8.