ClearanceBrief
510(k) K233006 ยท GZI Stimulator, Neuromuscular, External Functional

MyndMove, MyndMove 2.0

ApplicantMyndtec, Inc., Mississauga, CA
DecisionSubstantially Equivalent, Jun 25, 2024
ReceivedSep 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233006

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.