ClearanceBrief
510(k) K203735 ยท OBP Transcranial Magnetic Stimulator

Brainsway Deep TMS System

ApplicantBrainsway , Ltd., Jerusalem, IL
DecisionSubstantially Equivalent, Apr 23, 2021
ReceivedDec 21, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203735

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.