K-number	K092538
Device name	REFINE SUPPORT SYSTEM, MODEL 100.0100
Applicant	Alure Medical, Inc.
Product code	FTL
Device class	Class II
Decision date	Mar 5, 2010
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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REFINE SUPPORT SYSTEM, MODEL 100.0100

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