510(k) K050454 ยท FAS Electrode, Electrosurgical, Active, Urological
OMNITECH FULGURATING ELECTRODE
| Applicant | Omnitech Systems, Inc., Valparaiso IN, US |
| Decision | Substantially Equivalent, May 27, 2005 |
| Received | Feb 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050454
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.