K-number	K102590
Device name	FLEBOSET DOUBLE
Applicant	Laboratorios Grifols, S.A.
Product code	LHI
Device class	Class II
Decision date	Jan 13, 2011
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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FLEBOSET DOUBLE

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