AUDIBLE PRESSURE RELEASE VALVE WITH HUMIDIFIER ADAPTER / AND OXYGEN NIPPLE— 510(k) K111191

Name: FDA 510(k) clearance K111191
Creator: U.S. Food and Drug Administration
Published: 2011-07-28

Substantially Equivalent

Wet Nose Technologies, LLC

FDA 510(k) clearance K111191 for AUDIBLE PRESSURE RELEASE VALVE WITH HUMIDIFIER ADAPTER / AND OXYGEN NIPPLE, Substantially Equivalent on 2011-07-28. Applicant: Wet Nose Technologies, LLC. Device class: 2.

Clearance details

Applicant: Wet Nose Technologies, LLC
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 2011-04-28
Decision date: 2011-07-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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