K-number	K003889
Device name	ANCURE SHEATH MODEL # 40315, 40320, 40325
Applicant	Guidant Cardiac and Vascular Surgery
Product code	DYB
Device class	Class II
Decision date	Jan 24, 2002
Decision	Substantially Equivalent
Regulation	870.1340

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View the full FDA submission: accessdata.fda.gov

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ANCURE SHEATH MODEL # 40315, 40320, 40325

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