DEXIDE ENDO-LUBE KIT

DEXIDE ENDO-LUBE KIT is an FDA 510(k)-cleared medical device (K953611) manufactured by Dexide, Inc.. 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 September 14, 1995. Regulation: 8.