510(k) K203293 ยท GXD Generator, Lesion, Radiofrequency
Abbott Medical Grounding Pad, model RF-DGP-IS
| Applicant | ABBOTT MEDICAL, Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 21, 2022 |
| Received | Nov 9, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203293
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.