510(k) K781235

IV VITRO GAMMADAB T4 RIA KIT by Clinical Assays, Inc. — Product Code CDX

K781235 is an FDA 510(k) premarket notification submitted by Clinical Assays, Inc. for the device "IV VITRO GAMMADAB T4 RIA KIT". The FDA issued a decision of Substantially Equivalent on August 14, 1978. The device falls under product code CDX (Radioimmunoassay, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Clinical Assays, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 14, 1978
Date Received
July 19, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Total Thyroxine
Device Class
Class II
Regulation Number
862.1700
Review Panel
CH
Submission Type