K-number	K030962
Device name	DPX SERIES BRAVO DUO BONE DENSITOMETER
Applicant	Ge Lunar Corp.
Product code	KGI
Device class	Class II
Decision date	Jul 25, 2003
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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DPX SERIES BRAVO DUO BONE DENSITOMETER

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