510(k) K780361

T3 UPTAKE TEST by Monobind — Product Code KHQ

K780361 is an FDA 510(k) premarket notification submitted by Monobind for the device "T3 UPTAKE TEST". The FDA issued a decision of Substantially Equivalent on March 22, 1978. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Monobind has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 1978
Date Received
March 6, 1978
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