510(k) K935017 ยท JXE Device, Nerve Conduction Velocity Measurement
TD50 ELECTROMYOGRAPH
| Applicant | Medelec Intl. Corp., England, GB |
| Decision | Substantially Equivalent, Jul 28, 1994 |
| Received | Oct 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935017
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.