K-number	K071210
Device name	MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006
Applicant	Biomedical Diagnostics (Bmd) SA
Product code	LKO
Device class	Class II
Decision date	Dec 19, 2007
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006

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