K-number	K082391
Device name	PRIMAEVA MEDICAL RENESIS SYSTEM
Applicant	Primaeva Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	Sep 1, 2009
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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PRIMAEVA MEDICAL RENESIS SYSTEM

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