K-number	K090385
Device name	LARIAT II SUTURE DELIVERY DEVICE
Applicant	Sentreheart, Inc.
Product code	GAT
Device class	Class II
Decision date	May 6, 2009
Decision	Substantially Equivalent
Regulation	878.5000

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View the full FDA submission: accessdata.fda.gov

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LARIAT II SUTURE DELIVERY DEVICE

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