510(k) K210394 ยท FAS Electrode, Electrosurgical, Active, Urological
Electrosurgical accessory
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, May 19, 2021 |
| Received | Feb 10, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210394
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.