510(k) K061794

FIDIS TM THYRO, MODEL MX002 by Biomedical Diagnostics (Bmd) SA — Product Code JZO

K061794 is an FDA 510(k) premarket notification submitted by Biomedical Diagnostics (Bmd) SA for the device "FIDIS TM THYRO, MODEL MX002". The FDA issued a decision of Substantially Equivalent on November 21, 2006. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. Biomedical Diagnostics (Bmd) SA has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 2006
Date Received
June 26, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Thyroid Autoantibody
Device Class
Class II
Regulation Number
866.5870
Review Panel
IM
Submission Type