BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT

BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT is an FDA 510(k)-cleared medical device (K925173) manufactured by Westmed Intl.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 14, 1993. Regulation: 8.