GEMENI IGG ASSAY

Igg, Antigen, Antiserum, Control

ELECTRO-NUCLEONICS LABORATORIES, INC.

The following data is part of a premarket notification filed by Electro-nucleonics Laboratories, Inc. with the FDA for Gemeni Igg Assay.

Pre-market Notification Details

Device IDK800451
510k NumberK800451
Device Name:GEMENI IGG ASSAY
ClassificationIgg, Antigen, Antiserum, Control
Applicant ELECTRO-NUCLEONICS LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDEW  
CFR Regulation Number866.5510 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-02-29
Decision Date1980-04-24

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