
Airsonett, Inc.
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AIRSONNETT AIRSHOWER AIR 3 is an FDA 510(k)-cleared medical device (K081062) manufactured by Airsonett, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 2008. Regulation: 8.

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