K-number	K193517
Device name	ViziShot 2 FLEX
Applicant	Olympus Surgical Technologies America
Product code	KTI
Device class	Class II
Decision date	Mar 18, 2020
Decision	Substantially Equivalent
Regulation	874.4680

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Source

View the full FDA submission: accessdata.fda.gov

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ViziShot 2 FLEX

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