K-number	K901660
Device name	QUIDEL CHLAMYDIA TEST
Applicant	Quidel Corp.
Product code	LJC
Device class	Class I
Decision date	Jul 27, 1990
Decision	Substantially Equivalent
Regulation	866.3120

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View the full FDA submission: accessdata.fda.gov

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QUIDEL CHLAMYDIA TEST

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