K-number	K080715
Device name	ERBE VIO ESU, MODEL VIO 200 S
Applicant	Erbe USA, Inc.
Product code	GEI
Device class	Class II
Decision date	Apr 2, 2008
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ERBE VIO ESU, MODEL VIO 200 S

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