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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