K-number	K071573
Device name	RUGALIFT, MODEL# V.2.1
Applicant	Fatrotek S.R.L.
Product code	NFO
Device class	Class II
Decision date	Dec 9, 2008
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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RUGALIFT, MODEL# V.2.1

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