PERITONEAL DIALYSIS CATHETER

PERITONEAL DIALYSIS CATHETER is an FDA 510(k)-cleared medical device (K771555) manufactured by Fluoro-Mold Co.. 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 November 27, 1977. Regulation: 8.