510(k) K950314 ยท GXZ Electrode, Needle
DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)
| Applicant | Dantec Medical, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 25, 1996 |
| Received | Jan 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950314
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.