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U.S. Department of Health and Human Services

Product Classification

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Device plethysmograph, volume
Regulation Description Volume plethysmograph.
Regulation Medical Specialty Anesthesiology
Review Panel Anesthesiology
Product CodeJEH
Premarket Review Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1)
Division of Anesthesia, Respiratory, and Sleep Devices (DHT1C)
Submission Type 510(k)
Regulation Number 868.1760
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
Accredited Persons
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