SILASTIC ILEAL RESERVOIR CATHETER

SILASTIC ILEAL RESERVOIR CATHETER is an FDA 510(k)-cleared medical device (K760860) manufactured by Dow Corning Corp. Healthcare Industries Materials. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 22, 1976. Regulation: 8.