SODIUM CHLORIDE INHALATION SOLUTION, USP

SODIUM CHLORIDE INHALATION SOLUTION, USP is an FDA 510(k)-cleared medical device (K972466) 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 August 27, 1997. Regulation: 8.