510(k) K030526 ยท GWF Stimulator, Electrical, Evoked Response
PEDIGUARD NERVE DETECTOR SYSTEM
| Applicant | Spine Vision, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Dec 29, 2004 |
| Received | Feb 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030526
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.