K-number	K213593
Device name	OptiCross, OptiCross HD, OptiCross 6, OptiCross 6 HD
Applicant	Boston Scientific Corporation
Product code	OBJ
Device class	Class II
Decision date	Jan 14, 2022
Decision	Substantially Equivalent
Regulation	870.1200

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Source

View the full FDA submission: accessdata.fda.gov

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OptiCross, OptiCross HD, OptiCross 6, OptiCross 6 HD

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