Biomedical Diagnostics (Bmd) SA

FDA Regulatory Profile

Biomedical Diagnostics (Bmd) SA appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 3, 2010.

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K102607FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARISDecember 3, 2010
K100917FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEMNovember 3, 2010
K070458MODIFICATION TO FIDIS VASCULITIS, MODEL MX007December 21, 2007
K071210MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006December 19, 2007
K061794FIDIS TM THYRO, MODEL MX002November 21, 2006
K060380FIDIS DSDNAMay 2, 2006
K053383FIDIS CELIACMarch 29, 2006
K053653FIDIS CONNECTIVE 10, MODEL MX006March 13, 2006
K053012FIDIS VASCULITIS, MODEL MX007March 2, 2006
K050286FIDIS CONNECTIVE 8October 3, 2005