MARQUEST MICRO STIK 9000 SERIES

MARQUEST MICRO STIK 9000 SERIES is an FDA 510(k)-cleared medical device (K842008) manufactured by Marquest Medical Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 24, 1984. Regulation: 8.