K-number	K820340
Device name	T3 UPTAKE-SQUIBB DIAGNOSTIC KIT
Applicant	E. R. Squibb & Sons, Inc.
Product code	KHQ
Device class	Class II
Decision date	Mar 4, 1982
Decision	Substantially Equivalent
Regulation	862.1715

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View the full FDA submission: accessdata.fda.gov

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T3 UPTAKE-SQUIBB DIAGNOSTIC KIT

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