K-number	K981824
Device name	OPTICOAT T3 EIA KIT
Applicant	Biotecx Laboratories, Inc.
Product code	CDP
Device class	Class II
Decision date	Dec 22, 1998
Decision	Substantially Equivalent
Regulation	862.1710

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View the full FDA submission: accessdata.fda.gov

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OPTICOAT T3 EIA KIT

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