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FDA 510(k) Applications Submitted by COURIVAUD CHRISTELLE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050286
02/07/2005
FIDIS CONNECTIVE 8
BIOMEDICAL DIAGNOSTICS (BMD) SA
K070458
02/16/2007
MODIFICATION TO FIDIS VASCULITIS, MODEL MX007
BIOMEDICAL DIAGNOSTICS (BMD) SA
K100917
04/02/2010
FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM
BIOMEDICAL DIAGNOSTICS (BMD) SA
K071210
05/01/2007
MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006
BIOMEDICAL DIAGNOSTICS (BMD) SA
K102607
09/10/2010
FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARIS
BIOMEDICAL DIAGNOSTICS (BMD) SA
K053383
12/05/2005
FIDIS CELIAC
BIOMEDICAL DIAGNOSTICS (BMD) SA
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