K-number	K812231
Device name	INTRAVENOUS ADMINISTRATION SET
Applicant	Cordis Corp.
Product code	FPA
Device class	Class II
Decision date	Aug 20, 1981
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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INTRAVENOUS ADMINISTRATION SET

Everything you need for a 510(k) submission. Nothing you don't.