K-number	K940641
Device name	ELIAS ANA TOTAL
Applicant	Elias U.S.A., Inc.
Product code	LJM
Device class	Class II
Decision date	Mar 25, 1994
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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ELIAS ANA TOTAL

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