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U.S. Department of Health and Human Services

Product Classification

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Device lens, surgical, laser, accesssory, ophthalmic laser
Regulation Description Ophthalmic laser.
Regulation Medical Specialty Ophthalmic
Review Panel Ophthalmic
Product CodeLQJ
Premarket Review Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1)
Ophthalmic Devices (DHT1A)
Submission Type 510(k)
Regulation Number 886.4390
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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