510(k) K082614 ยท GWF Stimulator, Electrical, Evoked Response
EVOX ELECTRO DIAGNOSTIC DEVICE
| Applicant | Laborie Medical Technologies, Inc., Williston VT, US |
| Decision | Substantially Equivalent, Mar 6, 2009 |
| Received | Sep 9, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082614
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.