K-number	K920817
Device name	MODIFICATION PROSPECT GIARDIA RAPID ASSAY
Applicant	Alexon, Inc.
Product code	MHI
Device class	Class II
Decision date	Apr 22, 1992
Decision	Substantially Equivalent
Regulation	866.3220

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION PROSPECT GIARDIA RAPID ASSAY

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