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Ino Therapeutics, LLC
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INOMAX DS (DELIVERY SYSTEM), MODEL 10003 is an FDA 510(k)-cleared medical device (K070867) manufactured by Ino Therapeutics, LLC. 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 26, 2007. Regulation: 8.