DIALYZER, CAPILATORY, HOLLOW FIBER

DIALYZER, CAPILATORY, HOLLOW FIBER is an FDA 510(k)-cleared medical device (K772290) manufactured by Redy Laboratories. 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 March 14, 1978. Regulation: 8.