510(k) K915741 ยท GXE Leukotome
DISPOSABLE MONOPLAR MEDDLE ELECTRODES
| Applicant | Dantec Medical, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Dec 8, 1992 |
| Received | Dec 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915741
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.