ClearanceBrief
510(k) K190703 ยท GWF Stimulator, Electrical, Evoked Response

Neuro-IOM system with Neuro-IOM.NET software

ApplicantNeurosoft , Ltd., Ivanovo, RU
DecisionSubstantially Equivalent, May 22, 2021
ReceivedMar 18, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190703

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.