K-number	K063044
Device name	CARDIOBELT ELECTRODE BELT
Applicant	Monebo Technologies, Inc.
Product code	DRX
Device class	Class II
Decision date	Mar 23, 2007
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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CARDIOBELT ELECTRODE BELT

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