510(k) K013904 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BMC RADIO FREQUENCY PERFORATION GENERATOR, MODELS RFP-100-115 AND RFP-100-230
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Nov 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013904
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.