K-number	K884102
Device name	MODIFIED 7 INCH CONTINUOUS INFUSION SETS
Applicant	Quinton, Inc.
Product code	FPA
Device class	Class II
Decision date	Jan 31, 1989
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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MODIFIED 7 INCH CONTINUOUS INFUSION SETS

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