TRIEX-1 HOLLOW FIBER DIALYZER

TRIEX-1 HOLLOW FIBER DIALYZER is an FDA 510(k)-cleared medical device (K760781) manufactured by Extracorporeal Medical Specialities, 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 December 5, 1976. Regulation: 8.