K-number	K031087
Device name	EDWARDS INTRODUCER SHEATH
Applicant	Edwards Lifesciences, LLC
Product code	DYB
Device class	Class II
Decision date	Apr 24, 2003
Decision	Substantially Equivalent
Regulation	870.1340

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Source

View the full FDA submission: accessdata.fda.gov

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EDWARDS INTRODUCER SHEATH

Everything you need for a 510(k) submission. Nothing you don't.