Medical Device Manufacturer · US , Los Angeles , CA

Wet Nose Technologies, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Wet Nose Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Wet Nose Technologies, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Wet Nose Technologies, LLC
2 devices
1-2 of 2
Cleared Jul 28, 2011
AUDIBLE PRESSURE RELEASE VALVE WITH HUMIDIFIER ADAPTER / AND OXYGEN NIPPLE
K111191 · CBP
Anesthesiology · 91d
Cleared Mar 25, 2010
PRESSURE RELEASE VALVE W/AUDIBLE, MODEL PRV 20/40/60
K091538 · CBP
Anesthesiology · 303d
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