K-number	K821750
Device name	DESERET E-Z SET INFUSION SET
Applicant	Warner-Lambert Co.
Product code	FPA
Device class	Class II
Decision date	Jul 2, 1982
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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DESERET E-Z SET INFUSION SET

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