K-number	K943934
Device name	AORTIC ARCH CANNULAS
Applicant	Sorin Group Italia S.R.L.
Product code	DWF
Device class	Class II
Decision date	Jun 2, 1995
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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AORTIC ARCH CANNULAS

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