ClearanceBrief
510(k) K183303 ยท QCI Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder

Brainsway Deep TMS System

ApplicantBrainsway , Ltd., Jerusalem, IL
DecisionSubstantially Equivalent, Mar 8, 2019
ReceivedNov 27, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183303

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.