510(k) K222304 ยท KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Sonata Transcervical Fibroid Ablation System 2.2
| Applicant | Gynesonics, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Nov 8, 2022 |
| Received | Aug 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222304
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.