510(k) K203150 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Cool-tip RF Ablation System E Series
| Applicant | Covidien, LLC, Boulder CO, US |
| Decision | Substantially Equivalent, Feb 25, 2022 |
| Received | Oct 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203150
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.