510(k) K012069 ยท JXE Device, Nerve Conduction Velocity Measurement
MODIFICATION TO:BREVIO NERVE CONDUCTION TEST INSTRUMENT
| Applicant | Neurotron Medical, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, Aug 1, 2001 |
| Received | Jul 2, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012069
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.