510(k) K250275 · GEI Electrosurgical, Cutting & Coagulation & Accessories
PrecisePath Radiofrequency Puncture Generator and PrecisePath Footswitch
| Applicant | Baylis Medical Technologies, Inc., Mississauga, CA |
| Decision | Substantially Equivalent, Oct 28, 2025 |
| Received | Jan 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250275
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.