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U.S. Department of Health and Human Services

Product Classification
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Device ultrasound, sinus
Regulation Description Ultrasonic pulsed echo imaging system.
Regulation Medical Specialty Radiology
Review Panel Ear Nose & Throat
Product CodeLWI
Premarket Review Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1)
Division of Dental and ENT Devices (DHT1B)
Submission Type 510(k)
Regulation Number 892.1560
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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