510(k) K780539 ยท GWF Stimulator, Electrical, Evoked Response
STIMULATOR MODEL 8021
| Applicant | Life-Tech Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 22, 1978 |
| Received | Apr 3, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780539
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.