510(k) K101372 ยท GXI Probe, Radiofrequency Lesion
DUOCOOL PAIN MANAGEMENT PROBE, MODEL OSP-17-180-20
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Aug 10, 2010 |
| Received | May 17, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101372
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.