510(k) K013399 ยท HCC Device, Biofeedback
MODEL MES-9000/EMG SYSTEM
| Applicant | Myotronics-Noromed, Inc., Tukwila WA, US |
| Decision | Substantially Equivalent, Nov 13, 2001 |
| Received | Oct 15, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013399
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.