510(k) K071745 ยท GXI Probe, Radiofrequency Lesion
BAYLIS PAIN MANAGEMENT SINGLE-USE PROBE
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Jul 19, 2007 |
| Received | Jun 27, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071745
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.