510(k) K884663 ยท JXE Device, Nerve Conduction Velocity Measurement
IMPULSE EPIDURAL ELECTRODE
| Applicant | Impulse Systems, Inc., Madison WI, US |
| Decision | Substantially Equivalent, Jan 17, 1989 |
| Received | Nov 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884663
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.