K-number	K102425
Device name	ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM
Applicant	Zeus Scientific, Inc.
Product code	MID
Device class	Class II
Decision date	Dec 12, 2011
Decision	Substantially Equivalent
Regulation	866.5660

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View the full FDA submission: accessdata.fda.gov

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ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM

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