K-number	K082227
Device name	MINICAP HEMOGLOBIN(E) KIT, MODEL 2207, 2227
Applicant	Sebia
Product code	GKA
Device class	Class II
Decision date	Mar 26, 2009
Decision	Substantially Equivalent
Regulation	864.7415

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View the full FDA submission: accessdata.fda.gov

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MINICAP HEMOGLOBIN(E) KIT, MODEL 2207, 2227

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