K-number	K030209
Device name	MAHURKAR OPLUS CATHETER, MODEL 13.5 FR
Applicant	The Kendall Company
Product code	MPB
Device class	Class II
Decision date	May 13, 2003
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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MAHURKAR OPLUS CATHETER, MODEL 13.5 FR

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