ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX

ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX is an FDA 510(k)-cleared medical device (K083684) manufactured by Manufacturing & Research, 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 February 4, 2009. Regulation: 8.