510(k) K201610 ยท GXD Generator, Lesion, Radiofrequency
IonicRF Generator
| Applicant | ABBOTT MEDICAL, Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 21, 2020 |
| Received | Jun 15, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201610
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.