K-number	K121013
Device name	CONNEX VITAL SIGNS MONITOR 6000 SERIES
Applicant	Welch Allyn, Inc.
Product code	MWI
Device class	Class II
Decision date	Jul 26, 2012
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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CONNEX VITAL SIGNS MONITOR 6000 SERIES

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