510(k) K080159

KRONUS TSH RECEPTOR AUTOANTIBODY (TRAB) ELISA ASSAY KIT by Kronus Market Development Associates, Inc. — Product Code JZO

K080159 is an FDA 510(k) premarket notification submitted by Kronus Market Development Associates, Inc. for the device "KRONUS TSH RECEPTOR AUTOANTIBODY (TRAB) ELISA ASSAY KIT". The FDA issued a decision of Substantially Equivalent on May 22, 2008. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. Kronus Market Development Associates, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 2008
Date Received
January 23, 2008
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