510(k) K170708 ยท GXI Probe, Radiofrequency Lesion
OWL RF INSULATED CANNULAE
| Applicant | Diros Technology, Inc., Markham, CA |
| Decision | Substantially Equivalent, Jun 27, 2017 |
| Received | Mar 8, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170708
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.