510(k) K812666

THYROXINE (T4) 125I by Pcl-Ria, Inc. — Product Code CDP

K812666 is an FDA 510(k) premarket notification submitted by Pcl-Ria, Inc. for the device "THYROXINE (T4) 125I". The FDA issued a decision of Substantially Equivalent on October 2, 1981. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Pcl-Ria, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1981
Date Received
September 21, 1981
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