K-number	K180979
Device name	PureFlex Arterial Cannulae
Applicant	Sorin Group Italia S.R.L.
Product code	DWF
Device class	Class II
Decision date	Nov 16, 2018
Decision	Substantially Equivalent
Regulation	870.4210

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Source

View the full FDA submission: accessdata.fda.gov

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PureFlex Arterial Cannulae

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