510(k) K083391

THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY by Diagnostic Hybrids, Inc. — Product Code JZO

K083391 is an FDA 510(k) premarket notification submitted by Diagnostic Hybrids, Inc. for the device "THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY". The FDA issued a decision of Substantially Equivalent on May 21, 2009. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. Diagnostic Hybrids, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 21, 2009
Date Received
November 17, 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