K-number	K172586
Device name	Vios Monitoring System Model 2050
Applicant	Vios Medical, Inc.
Product code	DRT
Device class	Class II
Decision date	Jun 22, 2018
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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Vios Monitoring System Model 2050

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Vios Monitoring System Model 2050