510(k) K981824

OPTICOAT T3 EIA KIT by Biotecx Laboratories, Inc. — Product Code CDP

K981824 is an FDA 510(k) premarket notification submitted by Biotecx Laboratories, Inc. for the device "OPTICOAT T3 EIA KIT". The FDA issued a decision of Substantially Equivalent on December 22, 1998. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Biotecx Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 1998
Date Received
May 22, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Total Triiodothyronine
Device Class
Class II
Regulation Number
862.1710
Review Panel
CH
Submission Type