K-number	K081603
Device name	DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300
Applicant	Heartforce Medical, Inc.
Product code	DXR
Device class	Class II
Decision date	Jul 24, 2009
Decision	Substantially Equivalent
Regulation	870.2320

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View the full FDA submission: accessdata.fda.gov

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DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300

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