K-number	K012053
Device name	DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM
Applicant	Diamedix Corp.
Product code	MID
Device class	Class II
Decision date	Aug 20, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM

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