K-number	K052303
Device name	READMYHEART, MODEL RMH2.0
Applicant	Dailycare Biomedical, Inc.
Product code	DPS
Device class	Class II
Decision date	Dec 16, 2005
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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READMYHEART, MODEL RMH2.0

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