
Innomed Technologies, Inc./Respcare, Inc.
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NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBD is an FDA 510(k)-cleared medical device (K090804) manufactured by Innomed Technologies, Inc./Respcare, Inc.. 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 4, 2009. Regulation: 8.