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Ino Therapeutics
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INO THERAPEUTICS INOBLENDER, MODEL 10004 is an FDA 510(k)-cleared medical device (K052663) manufactured by Ino Therapeutics. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 3, 2005. Regulation: 8.