K-number	K162215
Device name	Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae
Applicant	Sorin Group Italia S.R.L.
Product code	DWF
Device class	Class II
Decision date	Jun 16, 2017
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae

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