K-number	K810211
Device name	T3 RIA KIT
Applicant	E. R. Squibb & Sons, Inc.
Product code	CDP
Device class	Class II
Decision date	Feb 10, 1981
Decision	Substantially Equivalent
Regulation	862.1710

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View the full FDA submission: accessdata.fda.gov

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T3 RIA KIT

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