K-number	K180456
Device name	Bio-Medicus Adult Cannulae Kit
Applicant	Medtronic, Inc.
Product code	DWF
Device class	Class II
Decision date	Mar 22, 2018
Decision	Substantially Equivalent
Regulation	870.4210

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Source

View the full FDA submission: accessdata.fda.gov

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Bio-Medicus Adult Cannulae Kit

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