K-number	K110953
Device name	VISENSIA, VISENSIA WITH ALERT
Applicant	Obs Medical
Product code	MHX
Device class	Class II
Decision date	Jun 15, 2011
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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VISENSIA, VISENSIA WITH ALERT

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