510(k) K002389 ยท GXI Probe, Radiofrequency Lesion
BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY
| Applicant | Baylis Medical Co., Inc., Mississauga, CA |
| Decision | Substantially Equivalent, Oct 23, 2000 |
| Received | Aug 4, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002389
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.