510(k) K100917

FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM by Biomedical Diagnostics (Bmd) SA — Product Code MOB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 3, 2010
Date Received
April 2, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
Device Class
Class II
Regulation Number
866.5660
Review Panel
IM
Submission Type