K-number	K150567
Device name	MEDTRONIC BIO-MEDICUS CANNULA INSERTION KIT
Applicant	Medtronic, Inc.
Product code	DWF
Device class	Class II
Decision date	Apr 9, 2015
Decision	Substantially Equivalent
Regulation	870.4210

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Source

View the full FDA submission: accessdata.fda.gov

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MEDTRONIC BIO-MEDICUS CANNULA INSERTION KIT

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