ADAPT OPEN ACCESS PORT, MODEL 41233

ADAPT OPEN ACCESS PORT, MODEL 41233 is an FDA 510(k)-cleared medical device (K021731) manufactured by Taut, 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 August 7, 2002. Regulation: 8.