510(k) K932533 ยท JXE Device, Nerve Conduction Velocity Measurement
SMARTSCOPE
| Applicant | Insight Medical Corp., Toronto, Ontario, CA |
| Decision | Substantially Equivalent, Mar 31, 1994 |
| Received | May 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932533
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.