LEECO T3% DIAGNOSTIC KIT

Radioassay, Triiodothyronine Uptake

LEECO DIAGNOSTICS, INC.

The following data is part of a premarket notification filed by Leeco Diagnostics, Inc. with the FDA for Leeco T3% Diagnostic Kit.

Pre-market Notification Details

Device IDK822575
510k NumberK822575
Device Name:LEECO T3% DIAGNOSTIC KIT
ClassificationRadioassay, Triiodothyronine Uptake
Applicant LEECO DIAGNOSTICS, INC. 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 Received1982-08-25
Decision Date1982-09-30

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