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U.S. Department of Health and Human Services

Product Classification
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Device tent, pediatric aerosol
Regulation Description Electrically powered oxygen tent.
Regulation Medical Specialty Anesthesiology
Review Panel Anesthesiology
Product CodeFNC
Premarket Review Division of Anesthesia, Respiratory, and Sleep Devices (DHT1C)
Division of Anesthesia, Respiratory, and Sleep Devices (DHT1C)
Submission Type 510(k)
Regulation Number 868.5710
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting		 Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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