510(k) K770918

LIQUI SOL T4 RIA TEST KIT by Damon Corp. — Product Code CDP

K770918 is an FDA 510(k) premarket notification submitted by Damon Corp. for the device "LIQUI SOL T4 RIA TEST KIT". The FDA issued a decision of Substantially Equivalent on June 17, 1977. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Damon Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 17, 1977
Date Received
May 19, 1977
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