PERITONEAL CATHETER STABILIZATION DEVICE 5C4381

PERITONEAL CATHETER STABILIZATION DEVICE 5C4381 is an FDA 510(k)-cleared medical device (K884554) manufactured by Baxter Healthcare Corp. 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 January 30, 1989. Regulation: 8.