510(k) K810482 ยท GWF Stimulator, Electrical, Evoked Response
SOMATOSENSORY STIMULATOR
| Applicant | Amplaid USA, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 29, 1981 |
| Received | Feb 23, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810482
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.