510(k) K170564 ยท GZI Stimulator, Neuromuscular, External Functional
MyndMove System, MyndMove Functional Electrical Stimulator
| Applicant | Myndtec, Inc., Mississauga, CA |
| Decision | Substantially Equivalent, Aug 30, 2017 |
| Received | Feb 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170564
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.