K-number	K132175
Device name	EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC CATHETER
Applicant	Edwards Lifesciences, LLC
Product code	DXC
Device class	Class II
Decision date	Sep 13, 2013
Decision	Substantially Equivalent
Regulation	870.4450

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View the full FDA submission: accessdata.fda.gov

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EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC CATHETER

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