K-number	K211965
Device name	StimRouter Neuromodulation System
Applicant	Bioness, Inc.
Product code	GZF
Device class	Class II
Decision date	Feb 23, 2022
Decision	Substantially Equivalent
Regulation	882.5870

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Source

View the full FDA submission: accessdata.fda.gov

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StimRouter Neuromodulation System

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