510(k) K851300 ยท GWF Stimulator, Electrical, Evoked Response
NEUROPACK 8, MEE-4108
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jun 13, 1985 |
| Received | Apr 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851300
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.