510(k) K173703 ยท KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Sonata Sonography-Guided Transcervical Fibroid Ablation System
| Applicant | Gynesonics, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 15, 2018 |
| Received | Dec 4, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173703
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.