Biomedical Diagnostics (Bmd) SA is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Biomedical Diagnostics (Bmd) SA - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Biomedical Diagnostics (Bmd) SA has 10 FDA 510(k) cleared immunology devices. Based in Marne La Vallee Cedex 2, FR.
Historical record: 10 cleared submissions from 2005 to 2010.
Browse the complete list of FDA 510(k) cleared immunology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomedical Diagnostics (Bmd) SA
10 devices
Cleared
Dec 03, 2010
FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARIS
Immunology
84d
Cleared
Nov 03, 2010
FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM
Immunology
215d
Cleared
Dec 21, 2007
MODIFICATION TO FIDIS VASCULITIS, MODEL MX007
Immunology
308d
Cleared
Dec 19, 2007
MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006
Immunology
232d
Cleared
Nov 21, 2006
FIDIS TM THYRO, MODEL MX002
Immunology
148d
Cleared
May 02, 2006
FIDIS DSDNA
Immunology
77d
Cleared
Mar 29, 2006
FIDIS CELIAC
Immunology
114d
Cleared
Mar 13, 2006
FIDIS CONNECTIVE 10, MODEL MX006
Immunology
73d
Cleared
Mar 02, 2006
FIDIS VASCULITIS, MODEL MX007
Immunology
127d
Cleared
Oct 03, 2005
FIDIS CONNECTIVE 8
Immunology
238d