K-number	K190823
Device name	Erbe ESU Model VIO 3 with Accessories
Applicant	Erbe Elektromedizin GmbH
Product code	GEI
Device class	Class II
Decision date	May 22, 2019
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Erbe ESU Model VIO 3 with Accessories

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