K-number	K001875
Device name	DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM
Applicant	Diamedix Corp.
Product code	LFX
Device class	Class II
Decision date	Aug 21, 2000
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM

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