510(k) K220122 ยท GXD Generator, Lesion, Radiofrequency
APEX 6
| Applicant | Rf Innovations, Inc., Middleton MA, US |
| Decision | Substantially Equivalent, Mar 15, 2023 |
| Received | Jan 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220122
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.