K-number	K122019
Device name	STREPTOCOCCUS APP. SEROLOGICAL REAGENTS
Applicant	Meridian Bioscience, Inc.
Product code	OYZ
Device class	Class I
Decision date	Sep 13, 2012
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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STREPTOCOCCUS APP. SEROLOGICAL REAGENTS

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