K-number	K920766
Device name	T4 EIA BEAD ASSAY
Applicant	Tech-Co, Inc.
Product code	CDX
Device class	Class II
Decision date	Apr 17, 1992
Decision	Substantially Equivalent
Regulation	862.1700

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View the full FDA submission: accessdata.fda.gov

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T4 EIA BEAD ASSAY

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