
Wet Nose Technologies, LLC
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AUDIBLE PRESSURE RELEASE VALVE WITH HUMIDIFIER ADAPTER / AND OXYGEN NIPPLE is an FDA 510(k)-cleared medical device (K111191) manufactured by Wet Nose Technologies, 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 July 27, 2011. Regulation: 8.