K-number	K092450
Device name	HUMAN IGD KIT FOR USE ON SPAPLUS
Applicant	The Binding Site
Product code	CZJ
Device class	Class II
Decision date	Dec 28, 2009
Decision	Substantially Equivalent
Regulation	866.5510

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Source

View the full FDA submission: accessdata.fda.gov

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HUMAN IGD KIT FOR USE ON SPAPLUS

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