K-number	K061794
Device name	FIDIS TM THYRO, MODEL MX002
Applicant	Biomedical Diagnostics (Bmd) SA
Product code	JZO
Device class	Class II
Decision date	Nov 21, 2006
Decision	Substantially Equivalent
Regulation	866.5870

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View the full FDA submission: accessdata.fda.gov

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FIDIS TM THYRO, MODEL MX002

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