STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL

STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBUL is an FDA 510(k)-cleared medical device (K901301) manufactured by Automatic Liquid Packaging, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 30, 1990. Regulation: 8.