510(k) K052407

ARCHITECT ANTI-TPO IMMUNOASSAY, CALIBRATORS & CONTROLS by Fisher Diagnostics — Product Code JZO

K052407 is an FDA 510(k) premarket notification submitted by Fisher Diagnostics for the device "ARCHITECT ANTI-TPO IMMUNOASSAY, CALIBRATORS & CONTROLS". The FDA issued a decision of Substantially Equivalent on July 18, 2006. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. Fisher Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 2006
Date Received
September 1, 2005
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