510(k) K820031 ยท JXE Device, Nerve Conduction Velocity Measurement
CADWELL 5200
| Applicant | Cadwell Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 4, 1982 |
| Received | Jan 6, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820031
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.