K-number	K021527
Device name	SECTRA OSTEOPOROSIS PACKAGE
Applicant	Sectra-Imtec AB
Product code	KGI
Device class	Class II
Decision date	Jun 7, 2002
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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SECTRA OSTEOPOROSIS PACKAGE

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