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U.S. Department of Health and Human Services

Product Classification
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Device implant, eye valve
Regulation Description Aqueous shunt.
Regulation Medical Specialty Ophthalmic
Review Panel Ophthalmic
Product CodeKYF
Premarket Review Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1)
Ophthalmic Devices (DHT1A)
Submission Type 510(k)
Regulation Number 886.3920
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting		 Ineligible
Implanted Device? Yes
Life-Sustain/Support Device? No
Recognized Consensus Standard
Third Party Review Not Third Party Eligible
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