510(k) K950208 ยท GWF Stimulator, Electrical, Evoked Response
NIHON KOHDEN NEUROPACK SIGMA MEB-5500A EVOKED RESPONSE & EMG MEASURING SYSTEM
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 10, 1995 |
| Received | Jan 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950208
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.