K-number	K153701
Device name	ULYSS Multi View Sinuscope
Applicant	Sopro-Comeg GmbH
Product code	EOB
Device class	Class II
Decision date	Sep 9, 2016
Decision	Substantially Equivalent
Regulation	874.4760

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View the full FDA submission: accessdata.fda.gov

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ULYSS Multi View Sinuscope

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