510(k) K151976 ยท FAS Electrode, Electrosurgical, Active, Urological
Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode
| Applicant | Omnitech Systems, Inc., Valparaiso IN, US |
| Decision | Substantially Equivalent, Jun 27, 2016 |
| Received | Jul 16, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151976
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.