510(k) K023342 ยท KOI Stimulator, Nerve, Peripheral, Electric
NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BG
| Applicant | Hdc Corp., Milpitas CA, US |
| Decision | Substantially Equivalent, Mar 2, 2004 |
| Received | Oct 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023342
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.