0.9.% SODIUM CHLORIDE INHALATION SOLUTION, USP

0.9.% SODIUM CHLORIDE INHALATION SOLUTION, USP is an FDA 510(k)-cleared medical device (K974056) manufactured by Holopack International, LP. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 20, 1998. Regulation: 8.