510(k) K083371 ยท GWF Stimulator, Electrical, Evoked Response
NAVIGATOR PRO WITH AEP SOFTWARE (BIOMARK, ENOG, CHAMP)
| Applicant | Natus Medical, Inc., Mudelein IL, US |
| Decision | Substantially Equivalent, Dec 8, 2009 |
| Received | Nov 14, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083371
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.