K-number	K072847
Device name	APEX 2.0 SOFTWARE FOR QDR X-RAY BONE DENSITOMETERS
Applicant	Hologic, Inc.
Product code	KGI
Device class	Class II
Decision date	Mar 28, 2008
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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APEX 2.0 SOFTWARE FOR QDR X-RAY BONE DENSITOMETERS

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