NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES

NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES is an FDA 510(k)-cleared medical device (K120182) manufactured by Neomed, 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 April 18, 2012. Regulation: 8.