510(k) K190259 ยท GXI Probe, Radiofrequency Lesion
Vesta RF Cannula
| Applicant | Biomerics, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 7, 2020 |
| Received | Feb 7, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190259
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.