510(k) K802243 ยท GXI Probe, Radiofrequency Lesion
VAXIOM FAMILY OF RF LESION PROBES & ELEC
| Applicant | Progress Mankind Technology, Hopkins MN, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Sep 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802243
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.