510(k) K223158 · GEI Electrosurgical, Cutting & Coagulation & Accessories
LigaSure XP Maryland Jaw Sealer/Divider
| Applicant | Covidien, LLC, Boulder CO, US |
| Decision | Substantially Equivalent, Jan 23, 2023 |
| Received | Oct 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223158
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.