K-number	K883999
Device name	QUIDEL GROUP A STREP TEST
Applicant	Quidel Corp.
Product code	GTZ
Device class	Class I
Decision date	Oct 12, 1988
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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QUIDEL GROUP A STREP TEST

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