K-number	K070488
Device name	MICARDIA ANNULOPLASTY BAND DR
Applicant	Micardia Corporation
Product code	KRH
Device class	Class II
Decision date	Sep 4, 2008
Decision	Substantially Equivalent
Regulation	870.3800

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View the full FDA submission: accessdata.fda.gov

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MICARDIA ANNULOPLASTY BAND DR

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