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U.S. Department of Health and Human Services

Product Classification

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Device keratome, battery-powered
Regulation Description Keratome.
Regulation Medical Specialty Ophthalmic
Review Panel Ophthalmic
Product CodeHMY
Premarket Review Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1)
Ophthalmic Devices (DHT1A)
Submission Type 510(k)
Regulation Number 886.4370
Device Class 1
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Guidance Document
Third Party Review
Accredited Persons
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