XPRESS MULTI-SINUS DILATION TOOL

XPRESS MULTI-SINUS DILATION TOOL is an FDA 510(k)-cleared medical device (K121174) manufactured by Entellus Medical, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 16, 2012. Regulation: 8.