510(k) K923676

VISTA THYROXINE UPTAKE ASSAY by Syva Co. — Product Code KHQ

K923676 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "VISTA THYROXINE UPTAKE ASSAY". The FDA issued a decision of Substantially Equivalent on October 9, 1992. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 9, 1992
Date Received
July 22, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioassay, Triiodothyronine Uptake
Device Class
Class II
Regulation Number
862.1715
Review Panel
CH
Submission Type