510(k) K150371 ยท GXI Probe, Radiofrequency Lesion
Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH
| Applicant | Diros Technology, Inc., Markham, CA |
| Decision | Substantially Equivalent, Jul 30, 2015 |
| Received | Feb 13, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150371
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.