510(k) K231327 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
POWERSEAL Sealer and Divider
| Applicant | Gyrus Acmi, Inc., Westborough MA, US |
| Decision | Substantially Equivalent, Oct 25, 2023 |
| Received | May 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231327
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.