510(k) K191073 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter
| Applicant | Vein 360, LLC, Blue Ash OH, US |
| Decision | Substantially Equivalent, Oct 22, 2019 |
| Received | Apr 22, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191073
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.