510(k) K121773 ยท GXI Probe, Radiofrequency Lesion
NIMBUS ELECTROSURGICAL RADIOFREQUENCY MULTITINED EXPANDABLE ELECTRODE
| Applicant | Biomerics, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 21, 2012 |
| Received | Jun 18, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121773
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.