K-number	K903194
Device name	REDITEST STREP A TEST KIT
Applicant	Boehringer Mannheim Corp.
Product code	GTZ
Device class	Class I
Decision date	Aug 22, 1990
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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REDITEST STREP A TEST KIT

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