K-number	K090999
Device name	BIOCARDIA MORPH SHEATH GUIDE
Applicant	Biocardia, Inc.
Product code	DYB
Device class	Class II
Decision date	Apr 15, 2009
Decision	Substantially Equivalent
Regulation	870.1340

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View the full FDA submission: accessdata.fda.gov

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BIOCARDIA MORPH SHEATH GUIDE

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