K-number	K141775
Device name	SOFIA (R) STREP A+ FIA
Applicant	Quidel Corporation
Product code	GTY
Device class	Class I
Decision date	Dec 16, 2014
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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SOFIA (R) STREP A+ FIA

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