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U.S. Department of Health and Human Services

Product Classification

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Device lens, multifocal intraocular
Regulation Description Intraocular lens.
Regulation Medical Specialty Ophthalmic
Review Panel Ophthalmic
Product CodeMFK
Premarket Review Ophthalmic Devices (DHT1A)
Ophthalmic Devices (DHT1A)
Submission Type PMA
Regulation Number 886.3600
Device Class 3
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? Yes
Life-Sustain/Support Device? No
Recognized Consensus Standards
Third Party Review Not Third Party Eligible
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