K-number	K071943
Device name	SERENITY PRO PSF SYSTEM
Applicant	Inolase 2002, Ltd.
Product code	GEX
Device class	Class II
Decision date	Aug 10, 2007
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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SERENITY PRO PSF SYSTEM

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