K-number	K964562
Device name	DTX-200 BONE DENSITOMETER
Applicant	Osteometer Meditech A/S
Product code	KGI
Device class	Class II
Decision date	Aug 22, 1997
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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DTX-200 BONE DENSITOMETER

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