FDA 510(k) Applications Submitted by CHRISTELLE COURIVAUD

FDA 510(k) Number Submission Date Device Name Applicant
K060380 02/14/2006 FIDIS DSDNA BIOMEDICAL DIAGNOSTICS (BMD) SA
K061794 06/26/2006 FIDIS TM THYRO, MODEL MX002 BIOMEDICAL DIAGNOSTICS (BMD) SA
K053012 10/26/2005 FIDIS VASCULITIS, MODEL MX007 BIOMEDICAL DIAGNOSTICS (BMD) SA
K053653 12/30/2005 FIDIS CONNECTIVE 10, MODEL MX006 BIOMEDICAL DIAGNOSTICS (BMD) SA


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