K-number	K080779
Device name	IRRISEPT WOUND CLEANSING SYSTEM
Applicant	Irrimax Corporation
Product code	FQH
Device class	Class II
Decision date	Feb 4, 2009
Decision	Substantially Equivalent
Regulation	880.5475

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View the full FDA submission: accessdata.fda.gov

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IRRISEPT WOUND CLEANSING SYSTEM

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