Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Biomedical Diagnostics (Bmd) SA

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K102607	FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARIS	LLL	2010-12-03	View
510(k)	K100917	FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM	MOB	2010-11-03	View
510(k)	K070458	MODIFICATION TO FIDIS VASCULITIS, MODEL MX007	MOB	2007-12-21	View
510(k)	K071210	MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006	LKO	2007-12-19	View
510(k)	K061794	FIDIS TM THYRO, MODEL MX002	JZO	2006-11-21	View
510(k)	K060380	FIDIS DSDNA	LSW	2006-05-02	View
510(k)	K053383	FIDIS CELIAC	MST	2006-03-29	View
510(k)	K053653	FIDIS CONNECTIVE 10, MODEL MX006	LLL	2006-03-13	View
510(k)	K053012	FIDIS VASCULITIS, MODEL MX007	MOB	2006-03-02	View
510(k)	K050286	FIDIS CONNECTIVE 8	LLL	2005-10-03	View

↑