K-number	K141951
Device name	DLP SILICONE CORONARY ARTERY OSTIAL CANNULAE
Applicant	Medtronic, Inc.
Product code	DWF
Device class	Class II
Decision date	Aug 15, 2014
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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DLP SILICONE CORONARY ARTERY OSTIAL CANNULAE

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