CORPAK GASTROSTOMY TUBE

CORPAK GASTROSTOMY TUBE is an FDA 510(k)-cleared medical device (K901501) manufactured by Corpak 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 June 10, 1990. Regulation: 8.