K-number	K832580
Device name	RAAF CATHETER REPAIR KIT
Applicant	Quinton, Inc.
Product code	LJS
Device class	Class II
Decision date	Jan 3, 1984
Decision	Substantially Equivalent
Regulation	880.5970

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Source

View the full FDA submission: accessdata.fda.gov

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RAAF CATHETER REPAIR KIT

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