510(k) K102566 ยท GXI Probe, Radiofrequency Lesion
OWL CANNULAE
| Applicant | Diros Technology, Inc., Markham, Ontario, CA |
| Decision | Substantially Equivalent, Jun 3, 2011 |
| Received | Sep 7, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102566
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.