K-number	K171404
Device name	BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)
Applicant	Bausch + Lomb, Incorporated
Product code	HQD
Device class	Class II
Decision date	Jul 17, 2017
Decision	Substantially Equivalent
Regulation	886.5916

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View the full FDA submission: accessdata.fda.gov

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BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)

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