T3 UPTAKE RADIOIMMUNOASSAY KIT

Radioassay, Triiodothyronine Uptake

TECHNIA DIAGNOSTICS LTD.

The following data is part of a premarket notification filed by Technia Diagnostics Ltd. with the FDA for T3 Uptake Radioimmunoassay Kit.

Pre-market Notification Details

Device IDK791361
510k NumberK791361
Device Name:T3 UPTAKE RADIOIMMUNOASSAY KIT
ClassificationRadioassay, Triiodothyronine Uptake
Applicant TECHNIA DIAGNOSTICS LTD. 803 N. Front St. Suite 3 McHenry,  IL  60050
Product CodeKHQ  
CFR Regulation Number862.1715 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-07-20
Decision Date1979-08-16

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