510(k) K965182 ยท GXD Generator, Lesion, Radiofrequency
RFG-3CF
| Applicant | Radionics, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Mar 12, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965182
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.