K-number	K042480
Device name	INFANT WHOLE BODY SOFTWARE OPTION FOR QDR DENSITOMETERS
Applicant	Hologic, Inc.
Product code	KGI
Device class	Class II
Decision date	Oct 29, 2004
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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INFANT WHOLE BODY SOFTWARE OPTION FOR QDR DENSITOMETERS

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