510(k) K203682 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Electrosurgical Generator ESG-400, Foot Switches, POWERSEAL Curved Jaw Sealer and Divider, Double Action
| Applicant | Olympus Winter & Ibe GmbH, Hamburg, DE |
| Decision | Substantially Equivalent, May 17, 2021 |
| Received | Dec 17, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203682
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.