K-number	K833749
Device name	PERITONEAL CATHETER-CHANGES-
Applicant	Quinton, Inc.
Product code	FKX
Device class	Class II
Decision date	Dec 27, 1983
Decision	Substantially Equivalent
Regulation	876.5630

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View the full FDA submission: accessdata.fda.gov

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PERITONEAL CATHETER-CHANGES-

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