K-number	K870318
Device name	AMEBIASIS ELISA TEST KIT
Applicant	Lmd Laboratories
Product code	KHW
Device class	Class II
Decision date	Aug 11, 1987
Decision	Substantially Equivalent
Regulation	866.3220

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View the full FDA submission: accessdata.fda.gov

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AMEBIASIS ELISA TEST KIT

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