K-number	K201632
Device name	TOMTEC-ARENA
Applicant	Tomtec Imaging Systems GmbH
Product code	LLZ
Device class	Class II
Decision date	Aug 14, 2020
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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TOMTEC-ARENA

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