K-number	K900973
Device name	VISUWELL(R) CHLAMYDIA
Applicant	Adi Diagnostics, Inc.
Product code	LJC
Device class	Class I
Decision date	May 15, 1990
Decision	Substantially Equivalent
Regulation	866.3120

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View the full FDA submission: accessdata.fda.gov

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VISUWELL(R) CHLAMYDIA

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