K-number	K855033
Device name	T-3 UPTAKE/RIASSAY
Applicant	Ria Diagnostics
Product code	KHQ
Device class	Class II
Decision date	Jan 24, 1986
Decision	Substantially Equivalent
Regulation	862.1715

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View the full FDA submission: accessdata.fda.gov

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T-3 UPTAKE/RIASSAY

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