510(k) K111687 ยท HCC Device, Biofeedback
EMG SYSTEM
| Applicant | Myotronics-Noromed, Inc., Kent WA, US |
| Decision | Substantially Equivalent, Sep 29, 2011 |
| Received | Jun 16, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111687
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.