510(k) K972190

THYROGLOBULIN ASSAY SYSTEM by American Laboratory Products Co., Ltd. — Product Code JZO

K972190 is an FDA 510(k) premarket notification submitted by American Laboratory Products Co., Ltd. for the device "THYROGLOBULIN ASSAY SYSTEM". The FDA issued a decision of Substantially Equivalent on July 14, 1997. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. American Laboratory Products Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1997
Date Received
May 19, 1997
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