510(k) K992439 ยท HCC Device, Biofeedback
NORODYN 8000 SEMG SYSTEM, ND-8000
| Applicant | Myotronics-Noromed, Inc., Tukwila WA, US |
| Decision | Substantially Equivalent, Aug 13, 1999 |
| Received | Jul 22, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992439
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.