NEMECTRODYN 8

Stimulator, Muscle, Powered

NEMECTRON MEDICAL, INC.

The following data is part of a premarket notification filed by Nemectron Medical, Inc. with the FDA for Nemectrodyn 8.

Pre-market Notification Details

Device IDK802804
510k NumberK802804
Device Name:NEMECTRODYN 8
ClassificationStimulator, Muscle, Powered
Applicant NEMECTRON MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIPF  
CFR Regulation Number890.5850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-11-05
Decision Date1981-03-16

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