510(k) K094054 ยท GWF Stimulator, Electrical, Evoked Response
MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, May 14, 2010 |
| Received | Dec 31, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K094054
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.