510(k) K103824

HUMAN IGA LIQUID REAGENT KIT FOR USE ON SPA PLUS by The Binding Site — Product Code CFN

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 27, 2012
Date Received
December 30, 2010
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Method, Nephelometric, Immunoglobulins (G, A, M)
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type