K-number	K922586
Device name	BARTELS RUBELLA IGG EIA
Applicant	Baxter Diagnostics, Inc.
Product code	LFX
Device class	Class II
Decision date	Sep 17, 1992
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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BARTELS RUBELLA IGG EIA

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