K-number	K870453
Device name	DS-DNA EIA DIAGNOSTIC KIT
Applicant	Biohytech International, Inc.
Product code	LJM
Device class	Class II
Decision date	Mar 24, 1987
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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DS-DNA EIA DIAGNOSTIC KIT

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