FDA 510(k) Applications Submitted by BIOMEDICAL DIAGNOSTICS (BMD) SA

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
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