K-number	K991066
Device name	MADTRONIC DLP ARTERIAL CANNULAE
Applicant	Medtronic Vascular
Product code	DWF
Device class	Class II
Decision date	Sep 14, 1999
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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MADTRONIC DLP ARTERIAL CANNULAE

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