K-number	K071826
Device name	THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910
Applicant	Fox Hollow Technologies
Product code	QEZ
Device class	Class II
Decision date	Nov 9, 2007
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910

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