K-number	K864949
Device name	INSTRUCTION CHANGE FOR RIGHT ATRIAL/RAAF CATHETER
Applicant	Quinton, Inc.
Product code	FOZ
Device class	Class II
Decision date	Feb 25, 1987
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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INSTRUCTION CHANGE FOR RIGHT ATRIAL/RAAF CATHETER

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