K-number	K082008
Device name	BIONET BM3PLUS PATIENT MONITOR
Applicant	Bionet Co., Ltd.
Product code	MWI
Device class	Class II
Decision date	Dec 11, 2008
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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BIONET BM3PLUS PATIENT MONITOR

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