K-number	K953671
Device name	ORGEN TEC ANTI-DSDNA ELISA ASSAY
Applicant	Orgentec
Product code	LRM
Device class	Class II
Decision date	Nov 9, 1995
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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ORGEN TEC ANTI-DSDNA ELISA ASSAY

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