K-number	K120169
Device name	INTERLAB IFE TEST USING G 26 VER. 2.0 INSTRUMENT
Applicant	Grifols USA, LLC
Product code	CFF
Device class	Class II
Decision date	Aug 24, 2012
Decision	Substantially Equivalent
Regulation	866.5510

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View the full FDA submission: accessdata.fda.gov

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INTERLAB IFE TEST USING G 26 VER. 2.0 INSTRUMENT

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