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Nephron Pharmaceuticals Corp.
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SODIUM CHLORIDE INHALATION SOLUTION, 3%, 7%, AND 10%, USP-4ML is an FDA 510(k)-cleared medical device (K120051) manufactured by Nephron Pharmaceuticals Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 2012. Regulation: 8.