510(k) K801203

CORTISOL RADIOIMMUNOASSAY KIT by Technia Diagnostics , Ltd. — Product Code CGR

K801203 is an FDA 510(k) premarket notification submitted by Technia Diagnostics , Ltd. for the device "CORTISOL RADIOIMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on June 9, 1980. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Technia Diagnostics , Ltd. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 1980
Date Received
May 19, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Cortisol
Device Class
Class II
Regulation Number
862.1205
Review Panel
CH
Submission Type