510(k) K202818 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Voyant Fine Fusion Device (EB230)
| Applicant | Applied Medical, Rancho Santa CA, US |
| Decision | Substantially Equivalent, Dec 16, 2021 |
| Received | Sep 24, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202818
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.