TRI-TUBE RIA

Radioassay, Triiodothyronine Uptake

NUCLEAR MEDICAL LABORATORIES, INC.

The following data is part of a premarket notification filed by Nuclear Medical Laboratories, Inc. with the FDA for Tri-tube Ria.

Pre-market Notification Details

Device IDK840589
510k NumberK840589
Device Name:TRI-TUBE RIA
ClassificationRadioassay, Triiodothyronine Uptake
Applicant NUCLEAR MEDICAL LABORATORIES, 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 Received1984-02-09
Decision Date1984-03-09

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