K-number	K020089
Device name	MAHURKAR TRIPLE LUMEN CATHETER, 12 FR
Applicant	The Kendall Company
Product code	NIE
Device class	Class II
Decision date	Apr 10, 2002
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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MAHURKAR TRIPLE LUMEN CATHETER, 12 FR

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