K-number	K002901
Device name	KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER
Applicant	The Kendall Company
Product code	MSD
Device class	Class II
Decision date	Mar 28, 2001
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

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