K-number	K190703
Device name	Neuro-IOM system with Neuro-IOM.NET software
Applicant	Neurosoft , Ltd.
Product code	GWF
Device class	Class II
Decision date	May 22, 2021
Decision	Substantially Equivalent
Regulation	882.1870

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View the full FDA submission: accessdata.fda.gov

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Neuro-IOM system with Neuro-IOM.NET software

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