K-number	K925355
Device name	BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST
Applicant	Princeton Biomedix
Product code	LFX
Device class	Class II
Decision date	Jul 12, 1994
Decision	Substantially Equivalent
Regulation	866.3510

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BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST

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