K-number	K182986
Device name	Boston Keratoprosthesis, Type I Lucia
Applicant	Massachusetts Eye and Ear Infirmary D/B/A Boston
Product code	HQM
Device class	Class II
Decision date	Jan 30, 2019
Decision	Substantially Equivalent
Regulation	886.3400

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Source

View the full FDA submission: accessdata.fda.gov

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Boston Keratoprosthesis, Type I Lucia

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