K-number	K110693
Device name	PACEART OPTIMA SYSTEM SOFTWARE
Applicant	Medtronic, Inc.
Product code	KRE
Device class	Class II
Decision date	Jun 8, 2011
Decision	Substantially Equivalent
Regulation	870.3640

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View the full FDA submission: accessdata.fda.gov

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PACEART OPTIMA SYSTEM SOFTWARE

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