K-number	K093976
Device name	RAISIN PERSONAL MONITOR
Applicant	Proteus Biomedical, Inc.
Product code	DXH
Device class	Class II
Decision date	Mar 25, 2010
Decision	Substantially Equivalent
Regulation	870.2920

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Source

View the full FDA submission: accessdata.fda.gov

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RAISIN PERSONAL MONITOR

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