BOUGIE, FILIFORM, JACKSON

BOUGIE, FILIFORM, JACKSON is an FDA 510(k)-cleared medical device (K770959) manufactured by V. Mueller O.V. Baxter Healthcare Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 13, 1977. Regulation: 8.