K-number	K132026
Device name	V SERIES MONITORING SYSTEM, 12.1 DCU/V12 AND 21.0 DCU/V21
Applicant	Mindray DS USA, Inc.
Product code	MHX
Device class	Class II
Decision date	Dec 20, 2013
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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V SERIES MONITORING SYSTEM, 12.1 DCU/V12 AND 21.0 DCU/V21

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