510(k) K092337 ยท GXI Probe, Radiofrequency Lesion
PAIN MANAGEMENT OPTIMA, MODEL PMO21-100-05, PMO20-100-10CS, PMO20-145-10CS
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Oct 16, 2009 |
| Received | Aug 4, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092337
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.